Canonical Allele Identifier: CA16602420
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 375941
dbSNP Id: rs121913227
COSMIC: COSM473

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753336_140753337delinsTT , CM000669.2:g.140753336_140753337delinsTT GRCh38
NC_000007.13:g.140453136_140453137delinsTT , CM000669.1:g.140453136_140453137delinsTT GRCh37
NC_000007.12:g.140099605_140099606delinsTT NCBI36
NG_007873.3:g.176428_176429delinsAA , LRG_299:g.176428_176429delinsAA

Transcript Alleles

HGVS Amino-acid change
ENST00000288602.11:c.1918_1919delinsAA ENSP00000288602.7:p.Val640Lys
ENST00000479537.6:n.468_469delinsAA
ENST00000496384.7:c.1798_1799delinsAA ENSP00000419060.2:p.Val600Lys
ENST00000497784.2:c.*1248_*1249delinsAA ENSP00000420119.2:p.=
ENST00000642228.1:c.*876_*877delinsAA ENSP00000493678.1:p.=
ENST00000642875.1:n.1259-3919_1259-3918delinsAA
ENST00000644120.1:n.2188_2189delinsAA
ENST00000644650.1:n.894_895delinsAA
ENST00000644905.1:n.2680_2681delinsAA
ENST00000644969.2:c.1918_1919delinsAA MANE Select ENSP00000496776.1:p.Val640Lys
ENST00000646730.1:c.*374_*375delinsAA ENSP00000494784.1:p.=
ENST00000646891.1:c.1798_1799delinsAA ENSP00000493543.1:p.Val600Lys
ENST00000647434.1:n.738-3919_738-3918delinsAA ENSP00000495132.1:p.=
ENST00000288602.10:c.1798_1799delinsAA ENSP00000288602.6:p.Val600Lys
ENST00000479537.5:n.82_83delinsAA ENSP00000418033.1:p.Val28Lys
ENST00000496384.6:n.621_622delinsAA
ENST00000497784.1:n.1833_1834delinsAA ENSP00000420119.1:p.=
NM_004333.4:c.1798_1799delinsAA , LRG_299t1:c.1798_1799delinsAA NP_004324.2:p.Val600Lys
XM_005250045.1:c.1798_1799delinsAA XP_005250102.1:p.Val600Lys
XM_005250046.1:c.1798_1799delinsAA XP_005250103.1:p.Val600Lys
XM_011516529.1:c.1798_1799delinsAA XP_011514831.1:p.Val600Lys
XM_011516530.1:c.1695-3919_1695-3918delinsAA XP_011514832.1:p.=
XR_242190.1:n.1806_1807delinsAA
XR_927520.1:n.1806_1807delinsAA
XR_927521.1:n.1806_1807delinsAA
XR_927522.1:n.1703-3919_1703-3918delinsAA
XR_927523.1:n.1703-3919_1703-3918delinsAA
NM_001354609.1:c.1798_1799delinsAA NP_001341538.1:p.Val600Lys
NM_004333.5:c.1798_1799delinsAA NP_004324.2:p.Val600Lys
NR_148928.1:n.2896_2897delinsAA
XM_017012558.1:c.1918_1919delinsAA XP_016868047.1:p.Val640Lys
XM_017012559.1:c.1918_1919delinsAA XP_016868048.1:p.Val640Lys
XR_001744857.1:n.1926_1927delinsAA
XR_001744858.1:n.1823-3919_1823-3918delinsAA
NM_001354609.2:c.1798_1799delinsAA NP_001341538.1:p.Val600Lys
NM_001374244.1:c.1918_1919delinsAA NP_001361173.1:p.Val640Lys
NM_001374258.1:c.1918_1919delinsAA MANE Select NP_001361187.1:p.Val640Lys
NM_004333.6:c.1798_1799delinsAA NP_004324.2:p.Val600Lys
NM_001378467.1:c.1807_1808delinsAA NP_001365396.1:p.Val603Lys
NM_001378468.1:c.1798_1799delinsAA NP_001365397.1:p.Val600Lys
NM_001378469.1:c.1732_1733delinsAA NP_001365398.1:p.Val578Lys
NM_001378470.1:c.1696_1697delinsAA NP_001365399.1:p.Val566Lys
NM_001378471.1:c.1687_1688delinsAA NP_001365400.1:p.Val563Lys
NM_001378472.1:c.1642_1643delinsAA NP_001365401.1:p.Val548Lys
NM_001378473.1:c.1642_1643delinsAA NP_001365402.1:p.Val548Lys
NM_001378474.1:c.1798_1799delinsAA NP_001365403.1:p.Val600Lys
NM_001378475.1:c.1534_1535delinsAA NP_001365404.1:p.Val512Lys