Canonical Allele Identifier: CA16042665
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 372671
ClinVar RCV Id: RCV000413723
dbSNP Id: rs1057517915

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140754202C>A , CM000669.2:g.140754202C>A GRCh38
NC_000007.13:g.140454002C>A , CM000669.1:g.140454002C>A GRCh37
NC_000007.12:g.140100471C>A NCBI36
NG_007873.3:g.175563G>T , LRG_299:g.175563G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000288602.11:c.1846G>T ENSP00000288602.7:p.Asp616Tyr
ENST00000479537.6:n.396G>T
ENST00000496384.7:c.1726G>T ENSP00000419060.2:p.Asp576Tyr
ENST00000497784.2:c.*1176G>T ENSP00000420119.2:p.=
ENST00000642228.1:c.*804G>T ENSP00000493678.1:p.=
ENST00000642875.1:n.1259-4784G>T
ENST00000644120.1:n.2116G>T
ENST00000644650.1:n.822G>T
ENST00000644905.1:n.1815G>T
ENST00000644969.2:c.1846G>T MANE Select ENSP00000496776.1:p.Asp616Tyr
ENST00000646730.1:c.*302G>T ENSP00000494784.1:p.=
ENST00000646891.1:c.1726G>T ENSP00000493543.1:p.Asp576Tyr
ENST00000647434.1:n.738-4784G>T ENSP00000495132.1:p.=
ENST00000288602.10:c.1726G>T ENSP00000288602.6:p.Asp576Tyr
ENST00000479537.5:n.10G>T ENSP00000418033.1:p.Asp4Tyr
ENST00000496384.6:n.549G>T
ENST00000497784.1:n.1761G>T ENSP00000420119.1:p.=
NM_004333.4:c.1726G>T , LRG_299t1:c.1726G>T NP_004324.2:p.Asp576Tyr
XM_005250045.1:c.1726G>T XP_005250102.1:p.Asp576Tyr
XM_005250046.1:c.1726G>T XP_005250103.1:p.Asp576Tyr
XM_011516529.1:c.1726G>T XP_011514831.1:p.Asp576Tyr
XM_011516530.1:c.1695-4784G>T XP_011514832.1:p.=
XR_242190.1:n.1734G>T
XR_927520.1:n.1734G>T
XR_927521.1:n.1734G>T
XR_927522.1:n.1703-4784G>T
XR_927523.1:n.1703-4784G>T
NM_001354609.1:c.1726G>T NP_001341538.1:p.Asp576Tyr
NM_004333.5:c.1726G>T NP_004324.2:p.Asp576Tyr
NR_148928.1:n.2031G>T
XM_017012558.1:c.1846G>T XP_016868047.1:p.Asp616Tyr
XM_017012559.1:c.1846G>T XP_016868048.1:p.Asp616Tyr
XR_001744857.1:n.1854G>T
XR_001744858.1:n.1823-4784G>T
NM_001354609.2:c.1726G>T NP_001341538.1:p.Asp576Tyr
NM_001374244.1:c.1846G>T NP_001361173.1:p.Asp616Tyr
NM_001374258.1:c.1846G>T MANE Select NP_001361187.1:p.Asp616Tyr
NM_004333.6:c.1726G>T NP_004324.2:p.Asp576Tyr
NM_001378467.1:c.1735G>T NP_001365396.1:p.Asp579Tyr
NM_001378468.1:c.1726G>T NP_001365397.1:p.Asp576Tyr
NM_001378469.1:c.1660G>T NP_001365398.1:p.Asp554Tyr
NM_001378470.1:c.1624G>T NP_001365399.1:p.Asp542Tyr
NM_001378471.1:c.1615G>T NP_001365400.1:p.Asp539Tyr
NM_001378472.1:c.1570G>T NP_001365401.1:p.Asp524Tyr
NM_001378473.1:c.1570G>T NP_001365402.1:p.Asp524Tyr
NM_001378474.1:c.1726G>T NP_001365403.1:p.Asp576Tyr
NM_001378475.1:c.1462G>T NP_001365404.1:p.Asp488Tyr