Canonical Allele Identifier: CA645544099
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs2128998293
COSMIC: COSM1127

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753336_140753338delinsCTC , CM000669.2:g.140753336_140753338delinsCTC GRCh38
NC_000007.13:g.140453136_140453138delinsCTC , CM000669.1:g.140453136_140453138delinsCTC GRCh37
NC_000007.12:g.140099605_140099607delinsCTC NCBI36
NG_007873.3:g.176427_176429delinsGAG , LRG_299:g.176427_176429delinsGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1797_1799delinsGAG MANE Select ENSP00000493543.1:p.Val600Arg
ENST00000288602.11:c.1917_1919delinsGAG ENSP00000288602.7:p.Val640Arg
ENST00000479537.6:c.467_469delinsGAG
ENST00000496384.7:c.1797_1799delinsGAG ENSP00000419060.2:p.Val600Arg
ENST00000497784.2:c.*1247_*1249delinsGAG ENSP00000420119.2:n.*1247_*1249delinsGAG
ENST00000642228.1:c.*875_*877delinsGAG ENSP00000493678.1:n.*875_*877delinsGAG
ENST00000642875.1:n.1259-3920_1259-3918delinsGAG
ENST00000644120.1:n.2187_2189delinsGAG
ENST00000644650.1:c.893_895delinsGAG
ENST00000644905.1:n.2679_2681delinsGAG
ENST00000644969.2:c.1917_1919delinsGAG MANE Plus Clinical ENSP00000496776.1:p.Val640Arg
ENST00000646730.1:c.*373_*375delinsGAG ENSP00000494784.1:n.*373_*375delinsGAG
ENST00000646891.1:c.1797_1799delinsGAG ENSP00000493543.1:p.Val600Arg
ENST00000647434.1:c.738-3920_738-3918delinsGAG ENSP00000495132.1:n.738-3920_738-3918delinsGAG
ENST00000288602.10:c.1797_1799delinsGAG ENSP00000288602.6:p.Val600Arg
ENST00000479537.5:c.81_83delinsGAG ENSP00000418033.1:p.Val28Arg
ENST00000496384.6:c.620_622delinsGAG
ENST00000497784.1:c.1832_1834delinsGAG ENSP00000420119.1:n.1832_1834delinsGAG
NM_004333.4:c.1797_1799delinsGAG , LRG_299t1:c.1797_1799delinsGAG NP_004324.2:p.Val600Arg
XM_005250045.1:c.1797_1799delinsGAG XP_005250102.1:p.Val600Arg
XM_005250046.1:c.1797_1799delinsGAG XP_005250103.1:p.Val600Arg
XM_011516529.1:c.1797_1799delinsGAG XP_011514831.1:p.Val600Arg
XM_011516530.1:c.1695-3920_1695-3918delinsGAG XP_011514832.1:n.1695-3920_1695-3918delinsGAG
XR_242190.1:n.1805_1807delinsGAG
XR_927520.1:n.1805_1807delinsGAG
XR_927521.1:n.1805_1807delinsGAG
XR_927522.1:n.1703-3920_1703-3918delinsGAG
XR_927523.1:n.1703-3920_1703-3918delinsGAG
NM_001354609.1:c.1797_1799delinsGAG NP_001341538.1:p.Val600Arg
NM_004333.5:c.1797_1799delinsGAG NP_004324.2:p.Val600Arg
NR_148928.1:n.2895_2897delinsGAG
XM_017012558.1:c.1917_1919delinsGAG XP_016868047.1:p.Val640Arg
XM_017012559.1:c.1917_1919delinsGAG XP_016868048.1:p.Val640Arg
XR_001744857.1:n.1925_1927delinsGAG
XR_001744858.1:n.1823-3920_1823-3918delinsGAG
NM_001354609.2:c.1797_1799delinsGAG NP_001341538.1:p.Val600Arg
NM_001374244.1:c.1917_1919delinsGAG NP_001361173.1:p.Val640Arg
NM_001374258.1:c.1917_1919delinsGAG MANE Plus Clinical NP_001361187.1:p.Val640Arg
NM_004333.6:c.1797_1799delinsGAG MANE Select NP_004324.2:p.Val600Arg
NM_001378467.1:c.1806_1808delinsGAG NP_001365396.1:p.Val603Arg
NM_001378468.1:c.1797_1799delinsGAG NP_001365397.1:p.Val600Arg
NM_001378469.1:c.1731_1733delinsGAG NP_001365398.1:p.Val578Arg
NM_001378470.1:c.1695_1697delinsGAG NP_001365399.1:p.Val566Arg
NM_001378471.1:c.1686_1688delinsGAG NP_001365400.1:p.Val563Arg
NM_001378472.1:c.1641_1643delinsGAG NP_001365401.1:p.Val548Arg
NM_001378473.1:c.1641_1643delinsGAG NP_001365402.1:p.Val548Arg
NM_001378474.1:c.1797_1799delinsGAG NP_001365403.1:p.Val600Arg
NM_001378475.1:c.1533_1535delinsGAG NP_001365404.1:p.Val512Arg