Canonical Allele Identifier: CA16021333
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375940
ClinVar RCV Id: RCV000440177
dbSNP Id: rs121913227
COSMIC: COSM474

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753336_140753337delinsCT , CM000669.2:g.140753336_140753337delinsCT GRCh38
NC_000007.13:g.140453136_140453137delinsCT , CM000669.1:g.140453136_140453137delinsCT GRCh37
NC_000007.12:g.140099605_140099606delinsCT NCBI36
NG_007873.3:g.176428_176429delinsAG , LRG_299:g.176428_176429delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000288602.11:c.1918_1919delinsAG ENSP00000288602.7:p.Val640Arg
ENST00000479537.6:n.468_469delinsAG
ENST00000496384.7:c.1798_1799delinsAG ENSP00000419060.2:p.Val600Arg
ENST00000497784.2:c.*1248_*1249delinsAG ENSP00000420119.2:p.=
ENST00000642228.1:c.*876_*877delinsAG ENSP00000493678.1:p.=
ENST00000642875.1:n.1259-3919_1259-3918delinsAG
ENST00000644120.1:n.2188_2189delinsAG
ENST00000644650.1:n.894_895delinsAG
ENST00000644905.1:n.2680_2681delinsAG
ENST00000644969.2:c.1918_1919delinsAG MANE Select ENSP00000496776.1:p.Val640Arg
ENST00000646730.1:c.*374_*375delinsAG ENSP00000494784.1:p.=
ENST00000646891.1:c.1798_1799delinsAG ENSP00000493543.1:p.Val600Arg
ENST00000647434.1:n.738-3919_738-3918delinsAG ENSP00000495132.1:p.=
ENST00000288602.10:c.1798_1799delinsAG ENSP00000288602.6:p.Val600Arg
ENST00000479537.5:n.82_83delinsAG ENSP00000418033.1:p.Val28Arg
ENST00000496384.6:n.621_622delinsAG
ENST00000497784.1:n.1833_1834delinsAG ENSP00000420119.1:p.=
NM_004333.4:c.1798_1799delinsAG , LRG_299t1:c.1798_1799delinsAG NP_004324.2:p.Val600Arg
XM_005250045.1:c.1798_1799delinsAG XP_005250102.1:p.Val600Arg
XM_005250046.1:c.1798_1799delinsAG XP_005250103.1:p.Val600Arg
XM_011516529.1:c.1798_1799delinsAG XP_011514831.1:p.Val600Arg
XM_011516530.1:c.1695-3919_1695-3918delinsAG XP_011514832.1:p.=
XR_242190.1:n.1806_1807delinsAG
XR_927520.1:n.1806_1807delinsAG
XR_927521.1:n.1806_1807delinsAG
XR_927522.1:n.1703-3919_1703-3918delinsAG
XR_927523.1:n.1703-3919_1703-3918delinsAG
NM_001354609.1:c.1798_1799delinsAG NP_001341538.1:p.Val600Arg
NM_004333.5:c.1798_1799delinsAG NP_004324.2:p.Val600Arg
NR_148928.1:n.2896_2897delinsAG
XM_017012558.1:c.1918_1919delinsAG XP_016868047.1:p.Val640Arg
XM_017012559.1:c.1918_1919delinsAG XP_016868048.1:p.Val640Arg
XR_001744857.1:n.1926_1927delinsAG
XR_001744858.1:n.1823-3919_1823-3918delinsAG
NM_001354609.2:c.1798_1799delinsAG NP_001341538.1:p.Val600Arg
NM_001374244.1:c.1918_1919delinsAG NP_001361173.1:p.Val640Arg
NM_001374258.1:c.1918_1919delinsAG MANE Select NP_001361187.1:p.Val640Arg
NM_004333.6:c.1798_1799delinsAG NP_004324.2:p.Val600Arg
NM_001378467.1:c.1807_1808delinsAG NP_001365396.1:p.Val603Arg
NM_001378468.1:c.1798_1799delinsAG NP_001365397.1:p.Val600Arg
NM_001378469.1:c.1732_1733delinsAG NP_001365398.1:p.Val578Arg
NM_001378470.1:c.1696_1697delinsAG NP_001365399.1:p.Val566Arg
NM_001378471.1:c.1687_1688delinsAG NP_001365400.1:p.Val563Arg
NM_001378472.1:c.1642_1643delinsAG NP_001365401.1:p.Val548Arg
NM_001378473.1:c.1642_1643delinsAG NP_001365402.1:p.Val548Arg
NM_001378474.1:c.1798_1799delinsAG NP_001365403.1:p.Val600Arg
NM_001378475.1:c.1534_1535delinsAG NP_001365404.1:p.Val512Arg