Canonical Allele Identifier: CA645544097
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs121913227
COSMIC: COSM249889

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753336_140753337delinsTG , CM000669.2:g.140753336_140753337delinsTG GRCh38
NC_000007.13:g.140453136_140453137delinsTG , CM000669.1:g.140453136_140453137delinsTG GRCh37
NC_000007.12:g.140099605_140099606delinsTG NCBI36
NG_007873.3:g.176428_176429delinsCA , LRG_299:g.176428_176429delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1798_1799delinsCA MANE Select ENSP00000493543.1:p.Val600Gln
ENST00000288602.11:c.1918_1919delinsCA ENSP00000288602.7:p.Val640Gln
ENST00000479537.6:c.468_469delinsCA
ENST00000496384.7:c.1798_1799delinsCA ENSP00000419060.2:p.Val600Gln
ENST00000497784.2:c.*1248_*1249delinsCA ENSP00000420119.2:n.*1248_*1249delinsCA
ENST00000642228.1:c.*876_*877delinsCA ENSP00000493678.1:n.*876_*877delinsCA
ENST00000642875.1:n.1259-3919_1259-3918delinsCA
ENST00000644120.1:n.2188_2189delinsCA
ENST00000644650.1:c.894_895delinsCA
ENST00000644905.1:n.2680_2681delinsCA
ENST00000644969.2:c.1918_1919delinsCA MANE Plus Clinical ENSP00000496776.1:p.Val640Gln
ENST00000646730.1:c.*374_*375delinsCA ENSP00000494784.1:n.*374_*375delinsCA
ENST00000646891.1:c.1798_1799delinsCA ENSP00000493543.1:p.Val600Gln
ENST00000647434.1:c.738-3919_738-3918delinsCA ENSP00000495132.1:n.738-3919_738-3918delinsCA
ENST00000288602.10:c.1798_1799delinsCA ENSP00000288602.6:p.Val600Gln
ENST00000479537.5:c.82_83delinsCA ENSP00000418033.1:p.Val28Gln
ENST00000496384.6:c.621_622delinsCA
ENST00000497784.1:c.1833_1834delinsCA ENSP00000420119.1:n.1833_1834delinsCA
NM_004333.4:c.1798_1799delinsCA , LRG_299t1:c.1798_1799delinsCA NP_004324.2:p.Val600Gln
XM_005250045.1:c.1798_1799delinsCA XP_005250102.1:p.Val600Gln
XM_005250046.1:c.1798_1799delinsCA XP_005250103.1:p.Val600Gln
XM_011516529.1:c.1798_1799delinsCA XP_011514831.1:p.Val600Gln
XM_011516530.1:c.1695-3919_1695-3918delinsCA XP_011514832.1:n.1695-3919_1695-3918delinsCA
XR_242190.1:n.1806_1807delinsCA
XR_927520.1:n.1806_1807delinsCA
XR_927521.1:n.1806_1807delinsCA
XR_927522.1:n.1703-3919_1703-3918delinsCA
XR_927523.1:n.1703-3919_1703-3918delinsCA
NM_001354609.1:c.1798_1799delinsCA NP_001341538.1:p.Val600Gln
NM_004333.5:c.1798_1799delinsCA NP_004324.2:p.Val600Gln
NR_148928.1:n.2896_2897delinsCA
XM_017012558.1:c.1918_1919delinsCA XP_016868047.1:p.Val640Gln
XM_017012559.1:c.1918_1919delinsCA XP_016868048.1:p.Val640Gln
XR_001744857.1:n.1926_1927delinsCA
XR_001744858.1:n.1823-3919_1823-3918delinsCA
NM_001354609.2:c.1798_1799delinsCA NP_001341538.1:p.Val600Gln
NM_001374244.1:c.1918_1919delinsCA NP_001361173.1:p.Val640Gln
NM_001374258.1:c.1918_1919delinsCA MANE Plus Clinical NP_001361187.1:p.Val640Gln
NM_004333.6:c.1798_1799delinsCA MANE Select NP_004324.2:p.Val600Gln
NM_001378467.1:c.1807_1808delinsCA NP_001365396.1:p.Val603Gln
NM_001378468.1:c.1798_1799delinsCA NP_001365397.1:p.Val600Gln
NM_001378469.1:c.1732_1733delinsCA NP_001365398.1:p.Val578Gln
NM_001378470.1:c.1696_1697delinsCA NP_001365399.1:p.Val566Gln
NM_001378471.1:c.1687_1688delinsCA NP_001365400.1:p.Val563Gln
NM_001378472.1:c.1642_1643delinsCA NP_001365401.1:p.Val548Gln
NM_001378473.1:c.1642_1643delinsCA NP_001365402.1:p.Val548Gln
NM_001378474.1:c.1798_1799delinsCA NP_001365403.1:p.Val600Gln
NM_001378475.1:c.1534_1535delinsCA NP_001365404.1:p.Val512Gln