Canonical Allele Identifier: CA457985467

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140439729T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739929T>G , CM000669.2:g.140739929T>G	GRCh38
NC_000007.13:g.140439729T>G , CM000669.1:g.140439729T>G	GRCh37
NC_000007.12:g.140086198T>G	NCBI36
NG_007873.3:g.189836A>C , LRG_299:g.189836A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.2010A>C MANE Select	ENSP00000493543.1:p.Gly670=
ENST00000288602.11:c.2130A>C	ENSP00000288602.7:p.Gly710=
ENST00000479537.6:c.762A>C
ENST00000496384.7:c.2010A>C	ENSP00000419060.2:p.Gly670=
ENST00000497784.2:c.*1460A>C	ENSP00000420119.2:n.*1460A>C
ENST00000642228.1:c.*1088A>C	ENSP00000493678.1:n.*1088A>C
ENST00000642875.1:n.1408A>C
ENST00000644120.1:n.2400A>C
ENST00000644650.1:c.1309A>C
ENST00000644905.1:n.2892A>C
ENST00000644969.2:c.2130A>C MANE Plus Clinical	ENSP00000496776.1:p.Gly710=
ENST00000645443.1:n.1789A>C
ENST00000646730.1:c.*668A>C	ENSP00000494784.1:n.*668A>C
ENST00000646891.1:c.2010A>C	ENSP00000493543.1:p.Gly670=
ENST00000647434.1:c.887A>C	ENSP00000495132.1:n.887A>C
ENST00000288602.10:c.2010A>C	ENSP00000288602.6:p.Gly670=
ENST00000479537.5:c.376A>C	ENSP00000418033.1:n.376A>C
ENST00000496384.6:c.833A>C
ENST00000497784.1:c.2045A>C	ENSP00000420119.1:n.2045A>C
NM_004333.4:c.2010A>C , LRG_299t1:c.2010A>C	NP_004324.2:p.Gly670=
XM_005250045.1:c.2010A>C	XP_005250102.1:p.Gly670=
XM_005250046.1:c.2010A>C	XP_005250103.1:p.Gly670=
XM_011516529.1:c.2010A>C	XP_011514831.1:p.Gly670=
XR_242190.1:n.2100A>C
XR_927520.1:n.2139A>C
XR_927521.1:n.2221A>C
XR_927522.1:n.1852A>C
XR_927523.1:n.1934A>C
NM_001354609.1:c.2010A>C	NP_001341538.1:p.Gly670=
NM_004333.5:c.2010A>C	NP_004324.2:p.Gly670=
NR_148928.1:n.3108A>C
XM_017012558.1:c.2130A>C	XP_016868047.1:p.Gly710=
XM_017012559.1:c.2130A>C	XP_016868048.1:p.Gly710=
XR_001744857.1:n.2220A>C
XR_001744858.1:n.1972A>C
NM_001354609.2:c.2010A>C	NP_001341538.1:p.Gly670=
NM_001374244.1:c.2130A>C	NP_001361173.1:p.Gly710=
NM_001374258.1:c.2130A>C MANE Plus Clinical	NP_001361187.1:p.Gly710=
NM_004333.6:c.2010A>C MANE Select	NP_004324.2:p.Gly670=
NM_001378467.1:c.2019A>C	NP_001365396.1:p.Gly673=
NM_001378468.1:c.2010A>C	NP_001365397.1:p.Gly670=
NM_001378469.1:c.1944A>C	NP_001365398.1:p.Gly648=
NM_001378470.1:c.1908A>C	NP_001365399.1:p.Gly636=
NM_001378471.1:c.1899A>C	NP_001365400.1:p.Gly633=
NM_001378472.1:c.1854A>C	NP_001365401.1:p.Gly618=
NM_001378473.1:c.1854A>C	NP_001365402.1:p.Gly618=
NM_001378474.1:c.2010A>C	NP_001365403.1:p.Gly670=
NM_001378475.1:c.1746A>C	NP_001365404.1:p.Gly582=