Canonical Allele Identifier: CA369590408

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140500216T>G (hg19) ; chr7:g.140800416T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140800416T>G , CM000669.2:g.140800416T>G	GRCh38
NC_000007.13:g.140500216T>G , CM000669.1:g.140500216T>G	GRCh37
NC_000007.12:g.140146685T>G	NCBI36
NG_007873.3:g.129349A>C , LRG_299:g.129349A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.926A>C MANE Select	ENSP00000493543.1:p.Glu309Ala
ENST00000288602.11:c.926A>C	ENSP00000288602.7:p.Glu309Ala
ENST00000496384.7:c.926A>C	ENSP00000419060.2:p.Glu309Ala
ENST00000497784.2:c.*376A>C	ENSP00000420119.2:n.*376A>C
ENST00000642228.1:c.*4A>C	ENSP00000493678.1:n.*4A>C
ENST00000642272.1:n.958A>C
ENST00000642875.1:n.420A>C
ENST00000644120.1:n.1368A>C
ENST00000644650.1:c.22A>C
ENST00000644905.1:n.1015A>C
ENST00000644969.2:c.926A>C MANE Plus Clinical	ENSP00000496776.1:p.Glu309Ala
ENST00000646730.1:c.926A>C	ENSP00000494784.1:p.Glu309Ala
ENST00000646891.1:c.926A>C	ENSP00000493543.1:p.Glu309Ala
ENST00000288602.10:c.926A>C	ENSP00000288602.6:p.Glu309Ala
ENST00000497784.1:c.961A>C	ENSP00000420119.1:n.961A>C
NM_004333.4:c.926A>C , LRG_299t1:c.926A>C	NP_004324.2:p.Glu309Ala
XM_005250045.1:c.926A>C	XP_005250102.1:p.Glu309Ala
XM_005250046.1:c.926A>C	XP_005250103.1:p.Glu309Ala
XM_011516529.1:c.926A>C	XP_011514831.1:p.Glu309Ala
XM_011516530.1:c.926A>C	XP_011514832.1:p.Glu309Ala
XR_242190.1:n.934A>C
XR_927520.1:n.934A>C
XR_927521.1:n.934A>C
XR_927522.1:n.934A>C
XR_927523.1:n.934A>C
NM_001354609.1:c.926A>C	NP_001341538.1:p.Glu309Ala
NM_004333.5:c.926A>C	NP_004324.2:p.Glu309Ala
NR_148928.1:n.1231A>C
XM_017012558.1:c.926A>C	XP_016868047.1:p.Glu309Ala
XM_017012559.1:c.926A>C	XP_016868048.1:p.Glu309Ala
XR_001744857.1:n.934A>C
XR_001744858.1:n.934A>C
NM_001354609.2:c.926A>C	NP_001341538.1:p.Glu309Ala
NM_001374244.1:c.926A>C	NP_001361173.1:p.Glu309Ala
NM_001374258.1:c.926A>C MANE Plus Clinical	NP_001361187.1:p.Glu309Ala
NM_004333.6:c.926A>C MANE Select	NP_004324.2:p.Glu309Ala
NM_001378467.1:c.935A>C	NP_001365396.1:p.Glu312Ala
NM_001378468.1:c.926A>C	NP_001365397.1:p.Glu309Ala
NM_001378469.1:c.926A>C	NP_001365398.1:p.Glu309Ala
NM_001378470.1:c.824A>C	NP_001365399.1:p.Glu275Ala
NM_001378471.1:c.926A>C	NP_001365400.1:p.Glu309Ala
NM_001378472.1:c.770A>C	NP_001365401.1:p.Glu257Ala
NM_001378473.1:c.770A>C	NP_001365402.1:p.Glu257Ala
NM_001378474.1:c.926A>C	NP_001365403.1:p.Glu309Ala
NM_001378475.1:c.662A>C	NP_001365404.1:p.Glu221Ala