Canonical Allele Identifier: CA369540976

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140449167C>A (hg19) ; chr7:g.140749367C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140749367C>A , CM000669.2:g.140749367C>A	GRCh38
NC_000007.13:g.140449167C>A , CM000669.1:g.140449167C>A	GRCh37
NC_000007.12:g.140095636C>A	NCBI36
NG_007873.3:g.180398G>T , LRG_299:g.180398G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1912G>T MANE Select	ENSP00000493543.1:p.Asp638Tyr
ENST00000288602.11:c.2032G>T	ENSP00000288602.7:p.Asp678Tyr
ENST00000479537.6:c.582G>T
ENST00000496384.7:c.1912G>T	ENSP00000419060.2:p.Asp638Tyr
ENST00000497784.2:c.*1362G>T	ENSP00000420119.2:n.*1362G>T
ENST00000642228.1:c.*990G>T	ENSP00000493678.1:n.*990G>T
ENST00000642875.1:n.1310G>T
ENST00000644120.1:n.2302G>T
ENST00000644650.1:c.1008G>T
ENST00000644905.1:n.2794G>T
ENST00000644969.2:c.2032G>T MANE Plus Clinical	ENSP00000496776.1:p.Asp678Tyr
ENST00000646730.1:c.*488G>T	ENSP00000494784.1:n.*488G>T
ENST00000646891.1:c.1912G>T	ENSP00000493543.1:p.Asp638Tyr
ENST00000647434.1:c.789G>T	ENSP00000495132.1:p.Gln263His
ENST00000288602.10:c.1912G>T	ENSP00000288602.6:p.Asp638Tyr
ENST00000479537.5:c.196G>T	ENSP00000418033.1:p.Asp66Tyr
ENST00000496384.6:c.735G>T
ENST00000497784.1:c.1947G>T	ENSP00000420119.1:n.1947G>T
NM_004333.4:c.1912G>T , LRG_299t1:c.1912G>T	NP_004324.2:p.Asp638Tyr
XM_005250045.1:c.1912G>T	XP_005250102.1:p.Asp638Tyr
XM_005250046.1:c.1912G>T	XP_005250103.1:p.Asp638Tyr
XM_011516529.1:c.1912G>T	XP_011514831.1:p.Asp638Tyr
XM_011516530.1:c.1746G>T	XP_011514832.1:p.Gln582His
XR_242190.1:n.1920G>T
XR_927520.1:n.1920G>T
XR_927521.1:n.1920G>T
XR_927522.1:n.1754G>T
XR_927523.1:n.1754G>T
NM_001354609.1:c.1912G>T	NP_001341538.1:p.Asp638Tyr
NM_004333.5:c.1912G>T	NP_004324.2:p.Asp638Tyr
NR_148928.1:n.3010G>T
XM_017012558.1:c.2032G>T	XP_016868047.1:p.Asp678Tyr
XM_017012559.1:c.2032G>T	XP_016868048.1:p.Asp678Tyr
XR_001744857.1:n.2040G>T
XR_001744858.1:n.1874G>T
NM_001354609.2:c.1912G>T	NP_001341538.1:p.Asp638Tyr
NM_001374244.1:c.2032G>T	NP_001361173.1:p.Asp678Tyr
NM_001374258.1:c.2032G>T MANE Plus Clinical	NP_001361187.1:p.Asp678Tyr
NM_004333.6:c.1912G>T MANE Select	NP_004324.2:p.Asp638Tyr
NM_001378467.1:c.1921G>T	NP_001365396.1:p.Asp641Tyr
NM_001378468.1:c.1912G>T	NP_001365397.1:p.Asp638Tyr
NM_001378469.1:c.1846G>T	NP_001365398.1:p.Asp616Tyr
NM_001378470.1:c.1810G>T	NP_001365399.1:p.Asp604Tyr
NM_001378471.1:c.1801G>T	NP_001365400.1:p.Asp601Tyr
NM_001378472.1:c.1756G>T	NP_001365401.1:p.Asp586Tyr
NM_001378473.1:c.1756G>T	NP_001365402.1:p.Asp586Tyr
NM_001378474.1:c.1912G>T	NP_001365403.1:p.Asp638Tyr
NM_001378475.1:c.1648G>T	NP_001365404.1:p.Asp550Tyr