Canonical Allele Identifier: CA1747718543

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781793G= , CM000669.2:g.140781793G=	GRCh38
NC_000007.13:g.140481593G= , CM000669.1:g.140481593G=	GRCh37
NC_000007.12:g.140128062G=	NCBI36
NG_007873.3:g.147972C= , LRG_299:g.147972C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1315-100C= MANE Select	ENSP00000493543.1:n.1315-100C=
ENST00000288602.11:c.1435-100C=	ENSP00000288602.7:n.1435-100C=
ENST00000496384.7:c.1315-100C=	ENSP00000419060.2:n.1315-100C=
ENST00000497784.2:c.*765-100C=	ENSP00000420119.2:n.*765-100C=
ENST00000642228.1:c.*393-100C=	ENSP00000493678.1:n.*393-100C=
ENST00000642875.1:n.757-100C=
ENST00000644120.1:n.1705-100C=
ENST00000644650.1:c.411-100C=
ENST00000644905.1:n.1404-100C=
ENST00000644969.2:c.1435-100C= MANE Plus Clinical	ENSP00000496776.1:n.1435-100C=
ENST00000646334.1:n.445-100C=
ENST00000646730.1:c.1315-100C=	ENSP00000494784.1:n.1315-100C=
ENST00000646891.1:c.1315-100C=	ENSP00000493543.1:n.1315-100C=
ENST00000647434.1:c.358-100C=	ENSP00000495132.1:n.358-100C=
ENST00000288602.10:c.1315-100C=	ENSP00000288602.6:n.1315-100C=
ENST00000496384.6:c.138-100C=
ENST00000497784.1:c.1350-100C=	ENSP00000420119.1:n.1350-100C=
NM_004333.4:c.1315-100C= , LRG_299t1:c.1315-100C=	NP_004324.2:n.1315-100C=
XM_005250045.1:c.1315-100C=	XP_005250102.1:n.1315-100C=
XM_005250046.1:c.1315-100C=	XP_005250103.1:n.1315-100C=
XM_011516529.1:c.1315-100C=	XP_011514831.1:n.1315-100C=
XM_011516530.1:c.1315-100C=	XP_011514832.1:n.1315-100C=
XR_242190.1:n.1323-100C=
XR_927520.1:n.1323-100C=
XR_927521.1:n.1323-100C=
XR_927522.1:n.1323-100C=
XR_927523.1:n.1323-100C=
NM_001354609.1:c.1315-100C=	NP_001341538.1:n.1315-100C=
NM_004333.5:c.1315-100C=	NP_004324.2:n.1315-100C=
NR_148928.1:n.1620-100C=
XM_017012558.1:c.1435-100C=	XP_016868047.1:n.1435-100C=
XM_017012559.1:c.1435-100C=	XP_016868048.1:n.1435-100C=
XR_001744857.1:n.1443-100C=
XR_001744858.1:n.1443-100C=
NM_001354609.2:c.1315-100C=	NP_001341538.1:n.1315-100C=
NM_001374244.1:c.1435-100C=	NP_001361173.1:n.1435-100C=
NM_001374258.1:c.1435-100C= MANE Plus Clinical	NP_001361187.1:n.1435-100C=
NM_004333.6:c.1315-100C= MANE Select	NP_004324.2:n.1315-100C=
NM_001378467.1:c.1324-100C=	NP_001365396.1:n.1324-100C=
NM_001378468.1:c.1315-100C=	NP_001365397.1:n.1315-100C=
NM_001378469.1:c.1249-100C=	NP_001365398.1:n.1249-100C=
NM_001378470.1:c.1213-100C=	NP_001365399.1:n.1213-100C=
NM_001378471.1:c.1204-100C=	NP_001365400.1:n.1204-100C=
NM_001378472.1:c.1159-100C=	NP_001365401.1:n.1159-100C=
NM_001378473.1:c.1159-100C=	NP_001365402.1:n.1159-100C=
NM_001378474.1:c.1315-100C=	NP_001365403.1:n.1315-100C=
NM_001378475.1:c.1051-100C=	NP_001365404.1:n.1051-100C=