Canonical Allele Identifier: CA1747710396
Gene: BRAF HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1726G= MANE Select ENSP00000493543.1:p.Asp576=
ENST00000288602.11:c.1846G= ENSP00000288602.7:p.Asp616=
ENST00000479537.6:c.396G=
ENST00000496384.7:c.1726G= ENSP00000419060.2:p.Asp576=
ENST00000497784.2:c.*1176G= ENSP00000420119.2:n.*1176G=
ENST00000642228.1:c.*804G= ENSP00000493678.1:n.*804G=
ENST00000642875.1:n.1259-4784G=
ENST00000644120.1:n.2116G=
ENST00000644650.1:c.822G=
ENST00000644905.1:n.1815G=
ENST00000644969.2:c.1846G= MANE Plus Clinical ENSP00000496776.1:p.Asp616=
ENST00000646730.1:c.*302G= ENSP00000494784.1:n.*302G=
ENST00000646891.1:c.1726G= ENSP00000493543.1:p.Asp576=
ENST00000647434.1:c.738-4784G= ENSP00000495132.1:n.738-4784G=
ENST00000288602.10:c.1726G= ENSP00000288602.6:p.Asp576=
ENST00000479537.5:c.10G= ENSP00000418033.1:p.Asp4=
ENST00000496384.6:c.549G=
ENST00000497784.1:c.1761G= ENSP00000420119.1:n.1761G=
NM_004333.4:c.1726G= , LRG_299t1:c.1726G= NP_004324.2:p.Asp576=
XM_005250045.1:c.1726G= XP_005250102.1:p.Asp576=
XM_005250046.1:c.1726G= XP_005250103.1:p.Asp576=
XM_011516529.1:c.1726G= XP_011514831.1:p.Asp576=
XM_011516530.1:c.1695-4784G= XP_011514832.1:n.1695-4784G=
XR_242190.1:n.1734G=
XR_927520.1:n.1734G=
XR_927521.1:n.1734G=
XR_927522.1:n.1703-4784G=
XR_927523.1:n.1703-4784G=
NM_001354609.1:c.1726G= NP_001341538.1:p.Asp576=
NM_004333.5:c.1726G= NP_004324.2:p.Asp576=
NR_148928.1:n.2031G=
XM_017012558.1:c.1846G= XP_016868047.1:p.Asp616=
XM_017012559.1:c.1846G= XP_016868048.1:p.Asp616=
XR_001744857.1:n.1854G=
XR_001744858.1:n.1823-4784G=
NM_001354609.2:c.1726G= NP_001341538.1:p.Asp576=
NM_001374244.1:c.1846G= NP_001361173.1:p.Asp616=
NM_001374258.1:c.1846G= MANE Plus Clinical NP_001361187.1:p.Asp616=
NM_004333.6:c.1726G= MANE Select NP_004324.2:p.Asp576=
NM_001378467.1:c.1735G= NP_001365396.1:p.Asp579=
NM_001378468.1:c.1726G= NP_001365397.1:p.Asp576=
NM_001378469.1:c.1660G= NP_001365398.1:p.Asp554=
NM_001378470.1:c.1624G= NP_001365399.1:p.Asp542=
NM_001378471.1:c.1615G= NP_001365400.1:p.Asp539=
NM_001378472.1:c.1570G= NP_001365401.1:p.Asp524=
NM_001378473.1:c.1570G= NP_001365402.1:p.Asp524=
NM_001378474.1:c.1726G= NP_001365403.1:p.Asp576=
NM_001378475.1:c.1462G= NP_001365404.1:p.Asp488=