Canonical Allele Identifier: CA645544091
Gene: BRAF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753332_140753338delinsATTCTCA , CM000669.2:g.140753332_140753338delinsATTCTCA GRCh38
NC_000007.13:g.140453132_140453138delinsATTCTCA , CM000669.1:g.140453132_140453138delinsATTCTCA GRCh37
NC_000007.12:g.140099601_140099607delinsATTCTCA NCBI36
NG_007873.3:g.176427_176433delinsTGAGAAT , LRG_299:g.176427_176433delinsTGAGAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1797_1803delinsTGAGAAT MANE Select ENSP00000493543.1:p.Val600_Lys601delinsGluAsn
ENST00000288602.11:c.1917_1923delinsTGAGAAT ENSP00000288602.7:p.Val640_Lys641delinsGluAsn
ENST00000479537.6:c.467_473delinsTGAGAAT
ENST00000496384.7:c.1797_1803delinsTGAGAAT ENSP00000419060.2:p.Val600_Lys601delinsGluAsn
ENST00000497784.2:c.*1247_*1253delinsTGAGAAT ENSP00000420119.2:n.*1247_*1253delinsTGAGAAT
ENST00000642228.1:c.*875_*881delinsTGAGAAT ENSP00000493678.1:n.*875_*881delinsTGAGAAT
ENST00000642875.1:n.1259-3920_1259-3914delinsTGAGAAT
ENST00000644120.1:n.2187_2193delinsTGAGAAT
ENST00000644650.1:c.893_899delinsTGAGAAT
ENST00000644905.1:n.2679_2685delinsTGAGAAT
ENST00000644969.2:c.1917_1923delinsTGAGAAT MANE Plus Clinical ENSP00000496776.1:p.Val640_Lys641delinsGluAsn
ENST00000646730.1:c.*373_*379delinsTGAGAAT ENSP00000494784.1:n.*373_*379delinsTGAGAAT
ENST00000646891.1:c.1797_1803delinsTGAGAAT ENSP00000493543.1:p.Val600_Lys601delinsGluAsn
ENST00000647434.1:c.738-3920_738-3914delinsTGAGAAT ENSP00000495132.1:n.738-3920_738-3914delinsTGAGAAT
ENST00000288602.10:c.1797_1803delinsTGAGAAT ENSP00000288602.6:p.Val600_Lys601delinsGluAsn
ENST00000479537.5:c.81_87delinsTGAGAAT ENSP00000418033.1:p.Val28_Lys29delinsGluAsn
ENST00000496384.6:c.620_626delinsTGAGAAT
ENST00000497784.1:c.1832_1838delinsTGAGAAT ENSP00000420119.1:n.1832_1838delinsTGAGAAT
NM_004333.4:c.1797_1803delinsTGAGAAT , LRG_299t1:c.1797_1803delinsTGAGAAT NP_004324.2:p.Val600_Lys601delinsGluAsn
XM_005250045.1:c.1797_1803delinsTGAGAAT XP_005250102.1:p.Val600_Lys601delinsGluAsn
XM_005250046.1:c.1797_1803delinsTGAGAAT XP_005250103.1:p.Val600_Lys601delinsGluAsn
XM_011516529.1:c.1797_1803delinsTGAGAAT XP_011514831.1:p.Val600_Lys601delinsGluAsn
XM_011516530.1:c.1695-3920_1695-3914delinsTGAGAAT XP_011514832.1:n.1695-3920_1695-3914delinsTGAGAAT
XR_242190.1:n.1805_1811delinsTGAGAAT
XR_927520.1:n.1805_1811delinsTGAGAAT
XR_927521.1:n.1805_1811delinsTGAGAAT
XR_927522.1:n.1703-3920_1703-3914delinsTGAGAAT
XR_927523.1:n.1703-3920_1703-3914delinsTGAGAAT
NM_001354609.1:c.1797_1803delinsTGAGAAT NP_001341538.1:p.Val600_Lys601delinsGluAsn
NM_004333.5:c.1797_1803delinsTGAGAAT NP_004324.2:p.Val600_Lys601delinsGluAsn
NR_148928.1:n.2895_2901delinsTGAGAAT
XM_017012558.1:c.1917_1923delinsTGAGAAT XP_016868047.1:p.Val640_Lys641delinsGluAsn
XM_017012559.1:c.1917_1923delinsTGAGAAT XP_016868048.1:p.Val640_Lys641delinsGluAsn
XR_001744857.1:n.1925_1931delinsTGAGAAT
XR_001744858.1:n.1823-3920_1823-3914delinsTGAGAAT
NM_001354609.2:c.1797_1803delinsTGAGAAT NP_001341538.1:p.Val600_Lys601delinsGluAsn
NM_001374244.1:c.1917_1923delinsTGAGAAT NP_001361173.1:p.Val640_Lys641delinsGluAsn
NM_001374258.1:c.1917_1923delinsTGAGAAT MANE Plus Clinical NP_001361187.1:p.Val640_Lys641delinsGluAsn
NM_004333.6:c.1797_1803delinsTGAGAAT MANE Select NP_004324.2:p.Val600_Lys601delinsGluAsn
NM_001378467.1:c.1806_1812delinsTGAGAAT NP_001365396.1:p.Val603_Lys604delinsGluAsn
NM_001378468.1:c.1797_1803delinsTGAGAAT NP_001365397.1:p.Val600_Lys601delinsGluAsn
NM_001378469.1:c.1731_1737delinsTGAGAAT NP_001365398.1:p.Val578_Lys579delinsGluAsn
NM_001378470.1:c.1695_1701delinsTGAGAAT NP_001365399.1:p.Val566_Lys567delinsGluAsn
NM_001378471.1:c.1686_1692delinsTGAGAAT NP_001365400.1:p.Val563_Lys564delinsGluAsn
NM_001378472.1:c.1641_1647delinsTGAGAAT NP_001365401.1:p.Val548_Lys549delinsGluAsn
NM_001378473.1:c.1641_1647delinsTGAGAAT NP_001365402.1:p.Val548_Lys549delinsGluAsn
NM_001378474.1:c.1797_1803delinsTGAGAAT NP_001365403.1:p.Val600_Lys601delinsGluAsn
NM_001378475.1:c.1533_1539delinsTGAGAAT NP_001365404.1:p.Val512_Lys513delinsGluAsn