Canonical Allele Identifier: CA369537968

Gene: BRAF

Linked Data

• dbSNP Id: rs2130899337
• MyVariant Identifiers: chr7:g.140439633A>T (hg19) ; chr7:g.140739833A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739833A>T , CM000669.2:g.140739833A>T	GRCh38
NC_000007.13:g.140439633A>T , CM000669.1:g.140439633A>T	GRCh37
NC_000007.12:g.140086102A>T	NCBI36
NG_007873.3:g.189932T>A , LRG_299:g.189932T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.2106T>A MANE Select	ENSP00000493543.1:p.Asp702Glu
ENST00000288602.11:c.2226T>A	ENSP00000288602.7:p.Asp742Glu
ENST00000479537.6:c.858T>A
ENST00000496384.7:c.2106T>A	ENSP00000419060.2:p.Asp702Glu
ENST00000497784.2:c.*1556T>A	ENSP00000420119.2:n.*1556T>A
ENST00000642228.1:c.*1184T>A	ENSP00000493678.1:n.*1184T>A
ENST00000642875.1:n.1504T>A
ENST00000644120.1:n.2496T>A
ENST00000644650.1:c.1405T>A
ENST00000644905.1:n.2988T>A
ENST00000644969.2:c.2226T>A MANE Plus Clinical	ENSP00000496776.1:p.Asp742Glu
ENST00000645443.1:n.1885T>A
ENST00000646730.1:c.*764T>A	ENSP00000494784.1:n.*764T>A
ENST00000646891.1:c.2106T>A	ENSP00000493543.1:p.Asp702Glu
ENST00000647434.1:c.983T>A	ENSP00000495132.1:n.983T>A
ENST00000288602.10:c.2106T>A	ENSP00000288602.6:p.Asp702Glu
ENST00000479537.5:c.472T>A	ENSP00000418033.1:n.472T>A
ENST00000496384.6:c.929T>A
ENST00000497784.1:c.2141T>A	ENSP00000420119.1:n.2141T>A
NM_004333.4:c.2106T>A , LRG_299t1:c.2106T>A	NP_004324.2:p.Asp702Glu
XM_005250045.1:c.2106T>A	XP_005250102.1:p.Asp702Glu
XM_005250046.1:c.2106T>A	XP_005250103.1:p.Asp702Glu
XM_011516529.1:c.2106T>A	XP_011514831.1:p.Asp702Glu
XR_242190.1:n.2196T>A
XR_927520.1:n.2235T>A
XR_927521.1:n.2317T>A
XR_927522.1:n.1948T>A
XR_927523.1:n.2030T>A
NM_001354609.1:c.2106T>A	NP_001341538.1:p.Asp702Glu
NM_004333.5:c.2106T>A	NP_004324.2:p.Asp702Glu
NR_148928.1:n.3204T>A
XM_017012558.1:c.2226T>A	XP_016868047.1:p.Asp742Glu
XM_017012559.1:c.2226T>A	XP_016868048.1:p.Asp742Glu
XR_001744857.1:n.2316T>A
XR_001744858.1:n.2068T>A
NM_001354609.2:c.2106T>A	NP_001341538.1:p.Asp702Glu
NM_001374244.1:c.2226T>A	NP_001361173.1:p.Asp742Glu
NM_001374258.1:c.2226T>A MANE Plus Clinical	NP_001361187.1:p.Asp742Glu
NM_004333.6:c.2106T>A MANE Select	NP_004324.2:p.Asp702Glu
NM_001378467.1:c.2115T>A	NP_001365396.1:p.Asp705Glu
NM_001378468.1:c.2106T>A	NP_001365397.1:p.Asp702Glu
NM_001378469.1:c.2040T>A	NP_001365398.1:p.Asp680Glu
NM_001378470.1:c.2004T>A	NP_001365399.1:p.Asp668Glu
NM_001378471.1:c.1995T>A	NP_001365400.1:p.Asp665Glu
NM_001378472.1:c.1950T>A	NP_001365401.1:p.Asp650Glu
NM_001378473.1:c.1950T>A	NP_001365402.1:p.Asp650Glu
NM_001378474.1:c.2106T>A	NP_001365403.1:p.Asp702Glu
NM_001378475.1:c.1842T>A	NP_001365404.1:p.Asp614Glu