Canonical Allele Identifier: CA1747732489

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140801445A= , CM000669.2:g.140801445A=	GRCh38
NC_000007.13:g.140501245A= , CM000669.1:g.140501245A=	GRCh37
NC_000007.12:g.140147714A=	NCBI36
NG_007873.3:g.128320T= , LRG_299:g.128320T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.827T= MANE Select	ENSP00000493543.1:p.Val276=
ENST00000288602.11:c.827T=	ENSP00000288602.7:p.Val276=
ENST00000496384.7:c.827T=	ENSP00000419060.2:p.Val276=
ENST00000497784.2:c.*277T=	ENSP00000420119.2:n.*277T=
ENST00000642228.1:c.827T=	ENSP00000493678.1:p.Val276=
ENST00000642272.1:n.859T=
ENST00000642875.1:n.321T=
ENST00000643356.1:n.428T=
ENST00000644120.1:n.1269T=
ENST00000644905.1:n.916T=
ENST00000644969.2:c.827T= MANE Plus Clinical	ENSP00000496776.1:p.Val276=
ENST00000646730.1:c.827T=	ENSP00000494784.1:p.Val276=
ENST00000646891.1:c.827T=	ENSP00000493543.1:p.Val276=
ENST00000288602.10:c.827T=	ENSP00000288602.6:p.Val276=
ENST00000497784.1:c.862T=	ENSP00000420119.1:n.862T=
NM_004333.4:c.827T= , LRG_299t1:c.827T=	NP_004324.2:p.Val276=
XM_005250045.1:c.827T=	XP_005250102.1:p.Val276=
XM_005250046.1:c.827T=	XP_005250103.1:p.Val276=
XM_011516529.1:c.827T=	XP_011514831.1:p.Val276=
XM_011516530.1:c.827T=	XP_011514832.1:p.Val276=
XR_242190.1:n.835T=
XR_927520.1:n.835T=
XR_927521.1:n.835T=
XR_927522.1:n.835T=
XR_927523.1:n.835T=
NM_001354609.1:c.827T=	NP_001341538.1:p.Val276=
NM_004333.5:c.827T=	NP_004324.2:p.Val276=
NR_148928.1:n.1132T=
XM_017012558.1:c.827T=	XP_016868047.1:p.Val276=
XM_017012559.1:c.827T=	XP_016868048.1:p.Val276=
XR_001744857.1:n.835T=
XR_001744858.1:n.835T=
NM_001354609.2:c.827T=	NP_001341538.1:p.Val276=
NM_001374244.1:c.827T=	NP_001361173.1:p.Val276=
NM_001374258.1:c.827T= MANE Plus Clinical	NP_001361187.1:p.Val276=
NM_004333.6:c.827T= MANE Select	NP_004324.2:p.Val276=
NM_001378467.1:c.836T=	NP_001365396.1:p.Val279=
NM_001378468.1:c.827T=	NP_001365397.1:p.Val276=
NM_001378469.1:c.827T=	NP_001365398.1:p.Val276=
NM_001378470.1:c.725T=	NP_001365399.1:p.Val242=
NM_001378471.1:c.827T=	NP_001365400.1:p.Val276=
NM_001378472.1:c.671T=	NP_001365401.1:p.Val224=
NM_001378473.1:c.671T=	NP_001365402.1:p.Val224=
NM_001378474.1:c.827T=	NP_001365403.1:p.Val276=
NM_001378475.1:c.563T=	NP_001365404.1:p.Val188=