View all transcripts

77 entries on 1 page. Showing entries 1 - 77.

ID     

Chr     

AscendingGene ID     

Name     

NCBI ID     

NCBI Protein ID     

Variants     
00000047 14 AKT1 transcript variant 3 NM_001014431.1 NP_001014431.1 0
00000062 2 ALK transcript variant 1 NM_004304.4 NP_004295.2 1
00000007 5 APC transcript variant 3 NM_000038.5 NP_000029.2 131
00000080 5 APC transcript variant 1 NM_001127511.2 NP_001120983.2 2
00000015 11 ATM ATM serine/threonine kinase NM_000051.3 NP_000042.3 162
00000033 3 BAP1 BRCA1 associated protein-1 (ubiquitin carboxy-terminal hydrolase) NM_004656.3 NP_004647.1 6
00000016 2 BARD1 transcript variant 1 NM_000465.3 NP_000456.2 51
00000049 15 BLM Bloom syndrome RecQ like helicase, transcript variant 1 NM_000057.3 NP_000048.1 1
00000017 10 BMPR1A bone morphogenetic protein receptor, type IA NM_004329.2 NP_004320.2 4
00000001 17 BRCA1 breast cancer 1, early onset, transcript variant 1 NM_007294.3 NP_009225.1 2788
00000002 13 BRCA2 breast cancer 2, early onset NM_000059.3 NP_000050.2 3086
00000018 17 BRIP1 BRCA1 interacting protein C-terminal helicase 1 NM_032043.2 NP_114432.2 73
00000019 16 CDH1 type 1, E-cadherin (epithelial) NM_004360.3 NP_004351.1 78
00000076 12 CDKN1B cyclin dependent kinase inhibitor 1B NM_004064.5 NP_004055.1 1
00000020 9 CDKN2A cyclin-dependent kinase inhibitor 2A, transcript variant 1 NM_000077.4 NP_000068.1 0
00000073 19 CEBPA transcript variant 1 NM_004364.4 NP_004355.2 3
00000040 22 CHEK2 transcript variant 1 NM_007194.3 NP_009125.1 26
00000044 22 CHEK2 transcript variant 3 NM_001005735.1 NP_001005735.1 17
00000074 5 CTNNA1 transcript variant 1 NM_001903.4 NP_001894.2 1
00000058 14 DICER1 transcript variant 1 NM_177438.2 NP_803187.1 2
00000059 14 DICER1 transcript variant 3 NM_001195573.1 NP_001182502.1 1
00000063 2 DIS3L2 transcript variant 1 NM_152383.4 NP_689596.4 2
00000066 1 EGLN1 egl-9 family hypoxia inducible factor 1 NM_022051.2 NP_071334.1 0
00000021 2 EPCAM epithelial cell adhesion molecule NM_002354.2 NP_002345.2 31
00000045 9 FANCC Fanconi anemia complementation group C, transcript variant 1 NM_000136.2 NP_000127.2 2
00000055 14 FANCM Fanconi anemia complementation group M, transcript variant 1 NM_020937.3 NP_065988.1 6
00000051 1 FH fumarate hydratase NM_000143.3 NP_000134.2 4
00000057 17 FLCN transcript variant 1 NM_144997.6 NP_659434.2 6
00000064 17 FLCN transcript variant 2 NM_144606.6 NP_653207.1 1
00000028 15 GREM1 transcript variant 1 NM_013372.6 NP_037504.1 0
00000067 1 KIF1B transcript variant 1 NM_015074.3 NP_055889.2 0
00000082 22 LZTR1 leucine zipper like transcription regulator 1 NM_006767.3 NP_006758.2 1
00000068 14 MAX transcript variant 1 NM_002382.4 NP_002373.3 0
00000056 7 MET transcript variant 1 NM_001127500.2 NP_001120972.1 9
00000032 3 MITF microphthalmia-associated transcription factor, transcript variant 4 NM_000248.3 NP_000239.1 0
00000003 3 MLH1 transcript variant 1 NM_000249.3 NP_000240.1 204
00000004 2 MSH2 transcript variant 1 NM_000251.2 NP_000242.1 168
00000005 2 MSH6 transcript variant 1 NM_000179.2 NP_000170.1 300
00000009 1 MUTYH mutY homolog, transcript variant alpha3 NM_001048171.1 NP_001041636.1 80
00000036 1 MUTYH mutY homolog, transcript variant alpha5 NM_001128425.1 NP_001121897.1 30
00000060 2 MYCN transcript variant 1 NM_001293228.2 NP_001280157.1 0
00000061 2 NBAS neuroblastoma amplified sequence, transcript variant 1 NM_015909.3 NP_056993.2 0
00000022 8 NBN nibrin NM_002485.4 NP_002476.2 79
00000030 17 NF1 transcript variant 2 NM_000267.3 NP_000258.1 17
00000034 22 NF2 neurofibromin 2 (merlin), transcript variant 1 NM_000268.3 NP_000259.1 2
00000041 16 PALB2 partner and localizer of BRCA2 NM_024675.3 NP_078951.2 64
00000079 4 PDGFRA transcript variant 1 NM_006206.5 NP_006197.1 1
00000014 2 PMS1 PMS1 postmeiotic segregation increased 1 (S. cerevisiae), transcript variant 1 NM_000534.4 NP_000525.1 0
00000010 7 PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae), transcript variant 1 NM_000535.5 NP_000526.1 263
00000027 19 POLD1 polymerase (DNA directed), delta 1, catalytic subunit, transcript variant 1 NM_001256849.1 NP_001243778.1 2
00000054 12 POLE DNA polymerase epsilon, catalytic subunit NM_006231.3 NP_006222.2 6
00000042 15 POLG polymerase (DNA directed), gamma, transcript variant 1 NM_002693.2 NP_002684.1 0
00000081 10 PTEN transcript variant 1 NM_000314.6 NP_000305.3 2
00000031 5 RAD50 RAD50 homolog (S. cerevisiae) NM_005732.3 NP_005723.2 4
00000024 17 RAD51C transcript variant 2 NM_002876.3 NP_002867.1 3
00000043 17 RAD51C transcript variant 1 NM_058216.2 NP_478123.1 2
00000025 17 RAD51D transcript variant 1 NM_002878.3 NP_002869.3 9
00000083 17 RAD51D transcript variant 6 NM_001142571.1 NP_001136043.1 1
00000077 13 RB1 RB transcriptional corepressor 1 NM_000321.2 NP_000312.2 1
00000052 12 RECQL transcript variant 2 NM_032941.2 NP_116559.1 1
00000046 10 RET transcript variant 2 NM_020975.5 NP_066124.1 9
00000048 10 RET transcript variant 4 NM_020630.5 NP_065681.1 2
00000069 5 SDHA transcript variant 1 NM_004168.3 NP_004159.2 1
00000070 11 SDHAF2 succinate dehydrogenase complex assembly factor 2 NM_017841.2 NP_060311.1 0
00000053 1 SDHB succinate dehydrogenase complex iron sulfur subunit B NM_003000.2 NP_002991.2 5
00000071 1 SDHC transcript variant 1 NM_003001.3 NP_002992.1 1
00000050 11 SDHD transcript variant 1 NM_003002.3 NP_002993.1 2
00000026 18 SMAD4 SMAD family member 4 NM_005359.5 NP_005350.1 3
00000065 15 SPRED1 sprouty related EVH1 domain containing 1 NM_152594.2 NP_689807.1 0
00000011 19 STK11 serine/threonine kinase 11 NM_000455.4 NP_000446.1 20
00000072 2 TMEM127 transcript variant 1 NM_017849.3 NP_060319.1 0
00000008 17 TP53 transcript variant 1 NM_000546.5 NP_000537.3 52
00000035 9 TSC1 transcript variant 1 NM_000368.4 NP_000359.1 4
00000037 16 TSC2 transcript variant 1 NM_000548.3 NP_000539.2 1
00000029 3 VHL E3 ubiquitin protein ligase, transcript variant 1 NM_000551.3 NP_000542.1 13
00000075 8 WRN Werner syndrome RecQ like helicase, transcript variant X1 XM_011544639.3 XP_011542941.1 3
00000078 11 WT1 Wilms tumor 1, transcript variant D NM_024426.5 NP_077744.4 1