Canonical Allele Identifier: CA1747710023
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753359T= , CM000669.2:g.140753359T= GRCh38
NC_000007.13:g.140453159T= , CM000669.1:g.140453159T= GRCh37
NC_000007.12:g.140099628T= NCBI36
NG_007873.3:g.176406A= , LRG_299:g.176406A=

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1776A= MANE Select ENSP00000493543.1:p.Ile592=
ENST00000288602.11:c.1896A= ENSP00000288602.7:p.Ile632=
ENST00000479537.6:c.446A=
ENST00000496384.7:c.1776A= ENSP00000419060.2:p.Ile592=
ENST00000497784.2:c.*1226A= ENSP00000420119.2:n.*1226A=
ENST00000642228.1:c.*854A= ENSP00000493678.1:n.*854A=
ENST00000642875.1:n.1259-3941A=
ENST00000644120.1:n.2166A=
ENST00000644650.1:c.872A=
ENST00000644905.1:n.2658A=
ENST00000644969.2:c.1896A= MANE Plus Clinical ENSP00000496776.1:p.Ile632=
ENST00000646730.1:c.*352A= ENSP00000494784.1:n.*352A=
ENST00000646891.1:c.1776A= ENSP00000493543.1:p.Ile592=
ENST00000647434.1:c.738-3941A= ENSP00000495132.1:n.738-3941A=
ENST00000288602.10:c.1776A= ENSP00000288602.6:p.Ile592=
ENST00000479537.5:c.60A= ENSP00000418033.1:p.Ile20=
ENST00000496384.6:c.599A=
ENST00000497784.1:c.1811A= ENSP00000420119.1:n.1811A=
NM_004333.4:c.1776A= , LRG_299t1:c.1776A= NP_004324.2:p.Ile592=
XM_005250045.1:c.1776A= XP_005250102.1:p.Ile592=
XM_005250046.1:c.1776A= XP_005250103.1:p.Ile592=
XM_011516529.1:c.1776A= XP_011514831.1:p.Ile592=
XM_011516530.1:c.1695-3941A= XP_011514832.1:n.1695-3941A=
XR_242190.1:n.1784A=
XR_927520.1:n.1784A=
XR_927521.1:n.1784A=
XR_927522.1:n.1703-3941A=
XR_927523.1:n.1703-3941A=
NM_001354609.1:c.1776A= NP_001341538.1:p.Ile592=
NM_004333.5:c.1776A= NP_004324.2:p.Ile592=
NR_148928.1:n.2874A=
XM_017012558.1:c.1896A= XP_016868047.1:p.Ile632=
XM_017012559.1:c.1896A= XP_016868048.1:p.Ile632=
XR_001744857.1:n.1904A=
XR_001744858.1:n.1823-3941A=
NM_001354609.2:c.1776A= NP_001341538.1:p.Ile592=
NM_001374244.1:c.1896A= NP_001361173.1:p.Ile632=
NM_001374258.1:c.1896A= MANE Plus Clinical NP_001361187.1:p.Ile632=
NM_004333.6:c.1776A= MANE Select NP_004324.2:p.Ile592=
NM_001378467.1:c.1785A= NP_001365396.1:p.Ile595=
NM_001378468.1:c.1776A= NP_001365397.1:p.Ile592=
NM_001378469.1:c.1710A= NP_001365398.1:p.Ile570=
NM_001378470.1:c.1674A= NP_001365399.1:p.Ile558=
NM_001378471.1:c.1665A= NP_001365400.1:p.Ile555=
NM_001378472.1:c.1620A= NP_001365401.1:p.Ile540=
NM_001378473.1:c.1620A= NP_001365402.1:p.Ile540=
NM_001378474.1:c.1776A= NP_001365403.1:p.Ile592=
NM_001378475.1:c.1512A= NP_001365404.1:p.Ile504=