Canonical Allele Identifier: CA369543271

Gene: BRAF

Linked Data

• dbSNP Id: rs121913335
• MyVariant Identifiers: chr7:g.140453175T>A (hg19) ; chr7:g.140753375T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1760A>T MANE Select	ENSP00000493543.1:p.Asp587Val
ENST00000288602.11:c.1880A>T	ENSP00000288602.7:p.Asp627Val
ENST00000479537.6:c.430A>T
ENST00000496384.7:c.1760A>T	ENSP00000419060.2:p.Asp587Val
ENST00000497784.2:c.*1210A>T	ENSP00000420119.2:n.*1210A>T
ENST00000642228.1:c.*838A>T	ENSP00000493678.1:n.*838A>T
ENST00000642875.1:n.1259-3957A>T
ENST00000644120.1:n.2150A>T
ENST00000644650.1:c.856A>T
ENST00000644905.1:n.2642A>T
ENST00000644969.2:c.1880A>T MANE Plus Clinical	ENSP00000496776.1:p.Asp627Val
ENST00000646730.1:c.*336A>T	ENSP00000494784.1:n.*336A>T
ENST00000646891.1:c.1760A>T	ENSP00000493543.1:p.Asp587Val
ENST00000647434.1:c.738-3957A>T	ENSP00000495132.1:n.738-3957A>T
ENST00000288602.10:c.1760A>T	ENSP00000288602.6:p.Asp587Val
ENST00000479537.5:c.44A>T	ENSP00000418033.1:p.Asp15Val
ENST00000496384.6:c.583A>T
ENST00000497784.1:c.1795A>T	ENSP00000420119.1:n.1795A>T
NM_004333.4:c.1760A>T , LRG_299t1:c.1760A>T	NP_004324.2:p.Asp587Val
XM_005250045.1:c.1760A>T	XP_005250102.1:p.Asp587Val
XM_005250046.1:c.1760A>T	XP_005250103.1:p.Asp587Val
XM_011516529.1:c.1760A>T	XP_011514831.1:p.Asp587Val
XM_011516530.1:c.1695-3957A>T	XP_011514832.1:n.1695-3957A>T
XR_242190.1:n.1768A>T
XR_927520.1:n.1768A>T
XR_927521.1:n.1768A>T
XR_927522.1:n.1703-3957A>T
XR_927523.1:n.1703-3957A>T
NM_001354609.1:c.1760A>T	NP_001341538.1:p.Asp587Val
NM_004333.5:c.1760A>T	NP_004324.2:p.Asp587Val
NR_148928.1:n.2858A>T
XM_017012558.1:c.1880A>T	XP_016868047.1:p.Asp627Val
XM_017012559.1:c.1880A>T	XP_016868048.1:p.Asp627Val
XR_001744857.1:n.1888A>T
XR_001744858.1:n.1823-3957A>T
NM_001354609.2:c.1760A>T	NP_001341538.1:p.Asp587Val
NM_001374244.1:c.1880A>T	NP_001361173.1:p.Asp627Val
NM_001374258.1:c.1880A>T MANE Plus Clinical	NP_001361187.1:p.Asp627Val
NM_004333.6:c.1760A>T MANE Select	NP_004324.2:p.Asp587Val
NM_001378467.1:c.1769A>T	NP_001365396.1:p.Asp590Val
NM_001378468.1:c.1760A>T	NP_001365397.1:p.Asp587Val
NM_001378469.1:c.1694A>T	NP_001365398.1:p.Asp565Val
NM_001378470.1:c.1658A>T	NP_001365399.1:p.Asp553Val
NM_001378471.1:c.1649A>T	NP_001365400.1:p.Asp550Val
NM_001378472.1:c.1604A>T	NP_001365401.1:p.Asp535Val
NM_001378473.1:c.1604A>T	NP_001365402.1:p.Asp535Val
NM_001378474.1:c.1760A>T	NP_001365403.1:p.Asp587Val
NM_001378475.1:c.1496A>T	NP_001365404.1:p.Asp499Val