Canonical Allele Identifier: CA135076
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40364
dbSNP Id: rs121913348
COSMIC: COSM450
CIViC: CA135076

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781617C>A , CM000669.2:g.140781617C>A GRCh38
NC_000007.13:g.140481417C>A , CM000669.1:g.140481417C>A GRCh37
NC_000007.12:g.140127886C>A NCBI36
NG_007873.3:g.148148G>T , LRG_299:g.148148G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000288602.11:c.1511G>T ENSP00000288602.7:p.Gly504Val
ENST00000479537.6:n.61G>T
ENST00000496384.7:c.1391G>T ENSP00000419060.2:p.Gly464Val
ENST00000497784.2:c.*841G>T ENSP00000420119.2:p.=
ENST00000642228.1:c.*469G>T ENSP00000493678.1:p.=
ENST00000642875.1:n.833G>T
ENST00000644120.1:n.1781G>T
ENST00000644650.1:n.487G>T
ENST00000644905.1:n.1480G>T
ENST00000644969.2:c.1511G>T MANE Select ENSP00000496776.1:p.Gly504Val
ENST00000646334.1:n.521G>T
ENST00000646730.1:c.1391G>T ENSP00000494784.1:p.Gly464Val
ENST00000646891.1:c.1391G>T ENSP00000493543.1:p.Gly464Val
ENST00000647434.1:n.434G>T ENSP00000495132.1:p.Gly145Val
ENST00000288602.10:c.1391G>T ENSP00000288602.6:p.Gly464Val
ENST00000496384.6:n.214G>T
ENST00000497784.1:n.1426G>T ENSP00000420119.1:p.=
NM_004333.4:c.1391G>T , LRG_299t1:c.1391G>T NP_004324.2:p.Gly464Val
XM_005250045.1:c.1391G>T XP_005250102.1:p.Gly464Val
XM_005250046.1:c.1391G>T XP_005250103.1:p.Gly464Val
XM_011516529.1:c.1391G>T XP_011514831.1:p.Gly464Val
XM_011516530.1:c.1391G>T XP_011514832.1:p.Gly464Val
XR_242190.1:n.1399G>T
XR_927520.1:n.1399G>T
XR_927521.1:n.1399G>T
XR_927522.1:n.1399G>T
XR_927523.1:n.1399G>T
NM_001354609.1:c.1391G>T NP_001341538.1:p.Gly464Val
NM_004333.5:c.1391G>T NP_004324.2:p.Gly464Val
NR_148928.1:n.1696G>T
XM_017012558.1:c.1511G>T XP_016868047.1:p.Gly504Val
XM_017012559.1:c.1511G>T XP_016868048.1:p.Gly504Val
XR_001744857.1:n.1519G>T
XR_001744858.1:n.1519G>T
NM_001354609.2:c.1391G>T NP_001341538.1:p.Gly464Val
NM_001374244.1:c.1511G>T NP_001361173.1:p.Gly504Val
NM_001374258.1:c.1511G>T MANE Select NP_001361187.1:p.Gly504Val
NM_004333.6:c.1391G>T NP_004324.2:p.Gly464Val
NM_001378467.1:c.1400G>T NP_001365396.1:p.Gly467Val
NM_001378468.1:c.1391G>T NP_001365397.1:p.Gly464Val
NM_001378469.1:c.1325G>T NP_001365398.1:p.Gly442Val
NM_001378470.1:c.1289G>T NP_001365399.1:p.Gly430Val
NM_001378471.1:c.1280G>T NP_001365400.1:p.Gly427Val
NM_001378472.1:c.1235G>T NP_001365401.1:p.Gly412Val
NM_001378473.1:c.1235G>T NP_001365402.1:p.Gly412Val
NM_001378474.1:c.1391G>T NP_001365403.1:p.Gly464Val
NM_001378475.1:c.1127G>T NP_001365404.1:p.Gly376Val