Canonical Allele Identifier: CA457985464

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140439726T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739926T>C , CM000669.2:g.140739926T>C	GRCh38
NC_000007.13:g.140439726T>C , CM000669.1:g.140439726T>C	GRCh37
NC_000007.12:g.140086195T>C	NCBI36
NG_007873.3:g.189839A>G , LRG_299:g.189839A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.2013A>G MANE Select	ENSP00000493543.1:p.Arg671=
ENST00000288602.11:c.2133A>G	ENSP00000288602.7:p.Arg711=
ENST00000479537.6:c.765A>G
ENST00000496384.7:c.2013A>G	ENSP00000419060.2:p.Arg671=
ENST00000497784.2:c.*1463A>G	ENSP00000420119.2:n.*1463A>G
ENST00000642228.1:c.*1091A>G	ENSP00000493678.1:n.*1091A>G
ENST00000642875.1:n.1411A>G
ENST00000644120.1:n.2403A>G
ENST00000644650.1:c.1312A>G
ENST00000644905.1:n.2895A>G
ENST00000644969.2:c.2133A>G MANE Plus Clinical	ENSP00000496776.1:p.Arg711=
ENST00000645443.1:n.1792A>G
ENST00000646730.1:c.*671A>G	ENSP00000494784.1:n.*671A>G
ENST00000646891.1:c.2013A>G	ENSP00000493543.1:p.Arg671=
ENST00000647434.1:c.890A>G	ENSP00000495132.1:n.890A>G
ENST00000288602.10:c.2013A>G	ENSP00000288602.6:p.Arg671=
ENST00000479537.5:c.379A>G	ENSP00000418033.1:n.379A>G
ENST00000496384.6:c.836A>G
ENST00000497784.1:c.2048A>G	ENSP00000420119.1:n.2048A>G
NM_004333.4:c.2013A>G , LRG_299t1:c.2013A>G	NP_004324.2:p.Arg671=
XM_005250045.1:c.2013A>G	XP_005250102.1:p.Arg671=
XM_005250046.1:c.2013A>G	XP_005250103.1:p.Arg671=
XM_011516529.1:c.2013A>G	XP_011514831.1:p.Arg671=
XR_242190.1:n.2103A>G
XR_927520.1:n.2142A>G
XR_927521.1:n.2224A>G
XR_927522.1:n.1855A>G
XR_927523.1:n.1937A>G
NM_001354609.1:c.2013A>G	NP_001341538.1:p.Arg671=
NM_004333.5:c.2013A>G	NP_004324.2:p.Arg671=
NR_148928.1:n.3111A>G
XM_017012558.1:c.2133A>G	XP_016868047.1:p.Arg711=
XM_017012559.1:c.2133A>G	XP_016868048.1:p.Arg711=
XR_001744857.1:n.2223A>G
XR_001744858.1:n.1975A>G
NM_001354609.2:c.2013A>G	NP_001341538.1:p.Arg671=
NM_001374244.1:c.2133A>G	NP_001361173.1:p.Arg711=
NM_001374258.1:c.2133A>G MANE Plus Clinical	NP_001361187.1:p.Arg711=
NM_004333.6:c.2013A>G MANE Select	NP_004324.2:p.Arg671=
NM_001378467.1:c.2022A>G	NP_001365396.1:p.Arg674=
NM_001378468.1:c.2013A>G	NP_001365397.1:p.Arg671=
NM_001378469.1:c.1947A>G	NP_001365398.1:p.Arg649=
NM_001378470.1:c.1911A>G	NP_001365399.1:p.Arg637=
NM_001378471.1:c.1902A>G	NP_001365400.1:p.Arg634=
NM_001378472.1:c.1857A>G	NP_001365401.1:p.Arg619=
NM_001378473.1:c.1857A>G	NP_001365402.1:p.Arg619=
NM_001378474.1:c.2013A>G	NP_001365403.1:p.Arg671=
NM_001378475.1:c.1749A>G	NP_001365404.1:p.Arg583=