Canonical Allele Identifier: CA369537959

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140439631T>G (hg19) ; chr7:g.140739831T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140739831T>G , CM000669.2:g.140739831T>G	GRCh38
NC_000007.13:g.140439631T>G , CM000669.1:g.140439631T>G	GRCh37
NC_000007.12:g.140086100T>G	NCBI36
NG_007873.3:g.189934A>C , LRG_299:g.189934A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.2108A>C MANE Select	ENSP00000493543.1:p.Glu703Ala
ENST00000288602.11:c.2228A>C	ENSP00000288602.7:p.Glu743Ala
ENST00000479537.6:c.860A>C
ENST00000496384.7:c.2108A>C	ENSP00000419060.2:p.Glu703Ala
ENST00000497784.2:c.*1558A>C	ENSP00000420119.2:n.*1558A>C
ENST00000642228.1:c.*1186A>C	ENSP00000493678.1:n.*1186A>C
ENST00000642875.1:n.1506A>C
ENST00000644120.1:n.2498A>C
ENST00000644650.1:c.1407A>C
ENST00000644905.1:n.2990A>C
ENST00000644969.2:c.2228A>C MANE Plus Clinical	ENSP00000496776.1:p.Glu743Ala
ENST00000645443.1:n.1887A>C
ENST00000646730.1:c.*766A>C	ENSP00000494784.1:n.*766A>C
ENST00000646891.1:c.2108A>C	ENSP00000493543.1:p.Glu703Ala
ENST00000647434.1:c.985A>C	ENSP00000495132.1:n.985A>C
ENST00000288602.10:c.2108A>C	ENSP00000288602.6:p.Glu703Ala
ENST00000479537.5:c.474A>C	ENSP00000418033.1:n.474A>C
ENST00000496384.6:c.931A>C
ENST00000497784.1:c.2143A>C	ENSP00000420119.1:n.2143A>C
NM_004333.4:c.2108A>C , LRG_299t1:c.2108A>C	NP_004324.2:p.Glu703Ala
XM_005250045.1:c.2108A>C	XP_005250102.1:p.Glu703Ala
XM_005250046.1:c.2108A>C	XP_005250103.1:p.Glu703Ala
XM_011516529.1:c.2108A>C	XP_011514831.1:p.Glu703Ala
XR_242190.1:n.2198A>C
XR_927520.1:n.2237A>C
XR_927521.1:n.2319A>C
XR_927522.1:n.1950A>C
XR_927523.1:n.2032A>C
NM_001354609.1:c.2108A>C	NP_001341538.1:p.Glu703Ala
NM_004333.5:c.2108A>C	NP_004324.2:p.Glu703Ala
NR_148928.1:n.3206A>C
XM_017012558.1:c.2228A>C	XP_016868047.1:p.Glu743Ala
XM_017012559.1:c.2228A>C	XP_016868048.1:p.Glu743Ala
XR_001744857.1:n.2318A>C
XR_001744858.1:n.2070A>C
NM_001354609.2:c.2108A>C	NP_001341538.1:p.Glu703Ala
NM_001374244.1:c.2228A>C	NP_001361173.1:p.Glu743Ala
NM_001374258.1:c.2228A>C MANE Plus Clinical	NP_001361187.1:p.Glu743Ala
NM_004333.6:c.2108A>C MANE Select	NP_004324.2:p.Glu703Ala
NM_001378467.1:c.2117A>C	NP_001365396.1:p.Glu706Ala
NM_001378468.1:c.2108A>C	NP_001365397.1:p.Glu703Ala
NM_001378469.1:c.2042A>C	NP_001365398.1:p.Glu681Ala
NM_001378470.1:c.2006A>C	NP_001365399.1:p.Glu669Ala
NM_001378471.1:c.1997A>C	NP_001365400.1:p.Glu666Ala
NM_001378472.1:c.1952A>C	NP_001365401.1:p.Glu651Ala
NM_001378473.1:c.1952A>C	NP_001365402.1:p.Glu651Ala
NM_001378474.1:c.2108A>C	NP_001365403.1:p.Glu703Ala
NM_001378475.1:c.1844A>C	NP_001365404.1:p.Glu615Ala