Canonical Allele Identifier: CA1747710029
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753375T= , CM000669.2:g.140753375T= GRCh38
NC_000007.13:g.140453175T= , CM000669.1:g.140453175T= GRCh37
NC_000007.12:g.140099644T= NCBI36
NG_007873.3:g.176390A= , LRG_299:g.176390A=

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1760A= MANE Select ENSP00000493543.1:p.Asp587=
ENST00000288602.11:c.1880A= ENSP00000288602.7:p.Asp627=
ENST00000479537.6:c.430A=
ENST00000496384.7:c.1760A= ENSP00000419060.2:p.Asp587=
ENST00000497784.2:c.*1210A= ENSP00000420119.2:n.*1210A=
ENST00000642228.1:c.*838A= ENSP00000493678.1:n.*838A=
ENST00000642875.1:n.1259-3957A=
ENST00000644120.1:n.2150A=
ENST00000644650.1:c.856A=
ENST00000644905.1:n.2642A=
ENST00000644969.2:c.1880A= MANE Plus Clinical ENSP00000496776.1:p.Asp627=
ENST00000646730.1:c.*336A= ENSP00000494784.1:n.*336A=
ENST00000646891.1:c.1760A= ENSP00000493543.1:p.Asp587=
ENST00000647434.1:c.738-3957A= ENSP00000495132.1:n.738-3957A=
ENST00000288602.10:c.1760A= ENSP00000288602.6:p.Asp587=
ENST00000479537.5:c.44A= ENSP00000418033.1:p.Asp15=
ENST00000496384.6:c.583A=
ENST00000497784.1:c.1795A= ENSP00000420119.1:n.1795A=
NM_004333.4:c.1760A= , LRG_299t1:c.1760A= NP_004324.2:p.Asp587=
XM_005250045.1:c.1760A= XP_005250102.1:p.Asp587=
XM_005250046.1:c.1760A= XP_005250103.1:p.Asp587=
XM_011516529.1:c.1760A= XP_011514831.1:p.Asp587=
XM_011516530.1:c.1695-3957A= XP_011514832.1:n.1695-3957A=
XR_242190.1:n.1768A=
XR_927520.1:n.1768A=
XR_927521.1:n.1768A=
XR_927522.1:n.1703-3957A=
XR_927523.1:n.1703-3957A=
NM_001354609.1:c.1760A= NP_001341538.1:p.Asp587=
NM_004333.5:c.1760A= NP_004324.2:p.Asp587=
NR_148928.1:n.2858A=
XM_017012558.1:c.1880A= XP_016868047.1:p.Asp627=
XM_017012559.1:c.1880A= XP_016868048.1:p.Asp627=
XR_001744857.1:n.1888A=
XR_001744858.1:n.1823-3957A=
NM_001354609.2:c.1760A= NP_001341538.1:p.Asp587=
NM_001374244.1:c.1880A= NP_001361173.1:p.Asp627=
NM_001374258.1:c.1880A= MANE Plus Clinical NP_001361187.1:p.Asp627=
NM_004333.6:c.1760A= MANE Select NP_004324.2:p.Asp587=
NM_001378467.1:c.1769A= NP_001365396.1:p.Asp590=
NM_001378468.1:c.1760A= NP_001365397.1:p.Asp587=
NM_001378469.1:c.1694A= NP_001365398.1:p.Asp565=
NM_001378470.1:c.1658A= NP_001365399.1:p.Asp553=
NM_001378471.1:c.1649A= NP_001365400.1:p.Asp550=
NM_001378472.1:c.1604A= NP_001365401.1:p.Asp535=
NM_001378473.1:c.1604A= NP_001365402.1:p.Asp535=
NM_001378474.1:c.1760A= NP_001365403.1:p.Asp587=
NM_001378475.1:c.1496A= NP_001365404.1:p.Asp499=