Canonical Allele Identifier: CA1747718363
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140781623C= , CM000669.2:g.140781623C= GRCh38
NC_000007.13:g.140481423C= , CM000669.1:g.140481423C= GRCh37
NC_000007.12:g.140127892C= NCBI36
NG_007873.3:g.148142G= , LRG_299:g.148142G=

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1385G= MANE Select ENSP00000493543.1:p.Arg462=
ENST00000288602.11:c.1505G= ENSP00000288602.7:p.Arg502=
ENST00000479537.6:c.55G=
ENST00000496384.7:c.1385G= ENSP00000419060.2:p.Arg462=
ENST00000497784.2:c.*835G= ENSP00000420119.2:n.*835G=
ENST00000642228.1:c.*463G= ENSP00000493678.1:n.*463G=
ENST00000642875.1:n.827G=
ENST00000644120.1:n.1775G=
ENST00000644650.1:c.481G=
ENST00000644905.1:n.1474G=
ENST00000644969.2:c.1505G= MANE Plus Clinical ENSP00000496776.1:p.Arg502=
ENST00000646334.1:n.515G=
ENST00000646730.1:c.1385G= ENSP00000494784.1:p.Arg462=
ENST00000646891.1:c.1385G= ENSP00000493543.1:p.Arg462=
ENST00000647434.1:c.428G= ENSP00000495132.1:p.Arg143=
ENST00000288602.10:c.1385G= ENSP00000288602.6:p.Arg462=
ENST00000496384.6:c.208G=
ENST00000497784.1:c.1420G= ENSP00000420119.1:n.1420G=
NM_004333.4:c.1385G= , LRG_299t1:c.1385G= NP_004324.2:p.Arg462=
XM_005250045.1:c.1385G= XP_005250102.1:p.Arg462=
XM_005250046.1:c.1385G= XP_005250103.1:p.Arg462=
XM_011516529.1:c.1385G= XP_011514831.1:p.Arg462=
XM_011516530.1:c.1385G= XP_011514832.1:p.Arg462=
XR_242190.1:n.1393G=
XR_927520.1:n.1393G=
XR_927521.1:n.1393G=
XR_927522.1:n.1393G=
XR_927523.1:n.1393G=
NM_001354609.1:c.1385G= NP_001341538.1:p.Arg462=
NM_004333.5:c.1385G= NP_004324.2:p.Arg462=
NR_148928.1:n.1690G=
XM_017012558.1:c.1505G= XP_016868047.1:p.Arg502=
XM_017012559.1:c.1505G= XP_016868048.1:p.Arg502=
XR_001744857.1:n.1513G=
XR_001744858.1:n.1513G=
NM_001354609.2:c.1385G= NP_001341538.1:p.Arg462=
NM_001374244.1:c.1505G= NP_001361173.1:p.Arg502=
NM_001374258.1:c.1505G= MANE Plus Clinical NP_001361187.1:p.Arg502=
NM_004333.6:c.1385G= MANE Select NP_004324.2:p.Arg462=
NM_001378467.1:c.1394G= NP_001365396.1:p.Arg465=
NM_001378468.1:c.1385G= NP_001365397.1:p.Arg462=
NM_001378469.1:c.1319G= NP_001365398.1:p.Arg440=
NM_001378470.1:c.1283G= NP_001365399.1:p.Arg428=
NM_001378471.1:c.1274G= NP_001365400.1:p.Arg425=
NM_001378472.1:c.1229G= NP_001365401.1:p.Arg410=
NM_001378473.1:c.1229G= NP_001365402.1:p.Arg410=
NM_001378474.1:c.1385G= NP_001365403.1:p.Arg462=
NM_001378475.1:c.1121G= NP_001365404.1:p.Arg374=