Canonical Allele Identifier: CA457985410

Gene: BRAF

Linked Data

• dbSNP Id: rs2130899356
• MyVariant Identifiers: chr7:g.140439636T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739836T>C , CM000669.2:g.140739836T>C	GRCh38
NC_000007.13:g.140439636T>C , CM000669.1:g.140439636T>C	GRCh37
NC_000007.12:g.140086105T>C	NCBI36
NG_007873.3:g.189929A>G , LRG_299:g.189929A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.2103A>G MANE Select	ENSP00000493543.1:p.Arg701=
ENST00000288602.11:c.2223A>G	ENSP00000288602.7:p.Arg741=
ENST00000479537.6:c.855A>G
ENST00000496384.7:c.2103A>G	ENSP00000419060.2:p.Arg701=
ENST00000497784.2:c.*1553A>G	ENSP00000420119.2:n.*1553A>G
ENST00000642228.1:c.*1181A>G	ENSP00000493678.1:n.*1181A>G
ENST00000642875.1:n.1501A>G
ENST00000644120.1:n.2493A>G
ENST00000644650.1:c.1402A>G
ENST00000644905.1:n.2985A>G
ENST00000644969.2:c.2223A>G MANE Plus Clinical	ENSP00000496776.1:p.Arg741=
ENST00000645443.1:n.1882A>G
ENST00000646730.1:c.*761A>G	ENSP00000494784.1:n.*761A>G
ENST00000646891.1:c.2103A>G	ENSP00000493543.1:p.Arg701=
ENST00000647434.1:c.980A>G	ENSP00000495132.1:n.980A>G
ENST00000288602.10:c.2103A>G	ENSP00000288602.6:p.Arg701=
ENST00000479537.5:c.469A>G	ENSP00000418033.1:n.469A>G
ENST00000496384.6:c.926A>G
ENST00000497784.1:c.2138A>G	ENSP00000420119.1:n.2138A>G
NM_004333.4:c.2103A>G , LRG_299t1:c.2103A>G	NP_004324.2:p.Arg701=
XM_005250045.1:c.2103A>G	XP_005250102.1:p.Arg701=
XM_005250046.1:c.2103A>G	XP_005250103.1:p.Arg701=
XM_011516529.1:c.2103A>G	XP_011514831.1:p.Arg701=
XR_242190.1:n.2193A>G
XR_927520.1:n.2232A>G
XR_927521.1:n.2314A>G
XR_927522.1:n.1945A>G
XR_927523.1:n.2027A>G
NM_001354609.1:c.2103A>G	NP_001341538.1:p.Arg701=
NM_004333.5:c.2103A>G	NP_004324.2:p.Arg701=
NR_148928.1:n.3201A>G
XM_017012558.1:c.2223A>G	XP_016868047.1:p.Arg741=
XM_017012559.1:c.2223A>G	XP_016868048.1:p.Arg741=
XR_001744857.1:n.2313A>G
XR_001744858.1:n.2065A>G
NM_001354609.2:c.2103A>G	NP_001341538.1:p.Arg701=
NM_001374244.1:c.2223A>G	NP_001361173.1:p.Arg741=
NM_001374258.1:c.2223A>G MANE Plus Clinical	NP_001361187.1:p.Arg741=
NM_004333.6:c.2103A>G MANE Select	NP_004324.2:p.Arg701=
NM_001378467.1:c.2112A>G	NP_001365396.1:p.Arg704=
NM_001378468.1:c.2103A>G	NP_001365397.1:p.Arg701=
NM_001378469.1:c.2037A>G	NP_001365398.1:p.Arg679=
NM_001378470.1:c.2001A>G	NP_001365399.1:p.Arg667=
NM_001378471.1:c.1992A>G	NP_001365400.1:p.Arg664=
NM_001378472.1:c.1947A>G	NP_001365401.1:p.Arg649=
NM_001378473.1:c.1947A>G	NP_001365402.1:p.Arg649=
NM_001378474.1:c.2103A>G	NP_001365403.1:p.Arg701=
NM_001378475.1:c.1839A>G	NP_001365404.1:p.Arg613=