Canonical Allele Identifier: CA135067
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40362
dbSNP Id: rs56101602
COSMIC: COSM1109

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781676C>T , CM000669.2:g.140781676C>T GRCh38
NC_000007.13:g.140481476C>T , CM000669.1:g.140481476C>T GRCh37
NC_000007.12:g.140127945C>T NCBI36
NG_007873.3:g.148089G>A , LRG_299:g.148089G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000288602.11:c.1452G>A ENSP00000288602.7:p.Arg484=
ENST00000479537.6:n.2G>A
ENST00000496384.7:c.1332G>A ENSP00000419060.2:p.Arg444=
ENST00000497784.2:c.*782G>A ENSP00000420119.2:p.=
ENST00000642228.1:c.*410G>A ENSP00000493678.1:p.=
ENST00000642875.1:n.774G>A
ENST00000644120.1:n.1722G>A
ENST00000644650.1:n.428G>A
ENST00000644905.1:n.1421G>A
ENST00000644969.2:c.1452G>A MANE Select ENSP00000496776.1:p.Arg484=
ENST00000646334.1:n.462G>A
ENST00000646730.1:c.1332G>A ENSP00000494784.1:p.Arg444=
ENST00000646891.1:c.1332G>A ENSP00000493543.1:p.Arg444=
ENST00000647434.1:n.375G>A ENSP00000495132.1:p.Arg125=
ENST00000288602.10:c.1332G>A ENSP00000288602.6:p.Arg444=
ENST00000496384.6:n.155G>A
ENST00000497784.1:n.1367G>A ENSP00000420119.1:p.=
NM_004333.4:c.1332G>A , LRG_299t1:c.1332G>A NP_004324.2:p.Arg444=
XM_005250045.1:c.1332G>A XP_005250102.1:p.Arg444=
XM_005250046.1:c.1332G>A XP_005250103.1:p.Arg444=
XM_011516529.1:c.1332G>A XP_011514831.1:p.Arg444=
XM_011516530.1:c.1332G>A XP_011514832.1:p.Arg444=
XR_242190.1:n.1340G>A
XR_927520.1:n.1340G>A
XR_927521.1:n.1340G>A
XR_927522.1:n.1340G>A
XR_927523.1:n.1340G>A
NM_001354609.1:c.1332G>A NP_001341538.1:p.Arg444=
NM_004333.5:c.1332G>A NP_004324.2:p.Arg444=
NR_148928.1:n.1637G>A
XM_017012558.1:c.1452G>A XP_016868047.1:p.Arg484=
XM_017012559.1:c.1452G>A XP_016868048.1:p.Arg484=
XR_001744857.1:n.1460G>A
XR_001744858.1:n.1460G>A
NM_001354609.2:c.1332G>A NP_001341538.1:p.Arg444=
NM_001374244.1:c.1452G>A NP_001361173.1:p.Arg484=
NM_001374258.1:c.1452G>A MANE Select NP_001361187.1:p.Arg484=
NM_004333.6:c.1332G>A NP_004324.2:p.Arg444=
NM_001378467.1:c.1341G>A NP_001365396.1:p.Arg447=
NM_001378468.1:c.1332G>A NP_001365397.1:p.Arg444=
NM_001378469.1:c.1266G>A NP_001365398.1:p.Arg422=
NM_001378470.1:c.1230G>A NP_001365399.1:p.Arg410=
NM_001378471.1:c.1221G>A NP_001365400.1:p.Arg407=
NM_001378472.1:c.1176G>A NP_001365401.1:p.Arg392=
NM_001378473.1:c.1176G>A NP_001365402.1:p.Arg392=
NM_001378474.1:c.1332G>A NP_001365403.1:p.Arg444=
NM_001378475.1:c.1068G>A NP_001365404.1:p.Arg356=