Canonical Allele Identifier: CA2260766460

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43057122A= , CM000679.2:g.43057122A=	GRCh38
NC_000017.10:g.41209139A= , CM000679.1:g.41209139A=	GRCh37
NC_000017.9:g.38462665A=	NCBI36
NG_005905.2:g.160862T= , LRG_292:g.160862T=

Transcript Alleles

HGVS	Amino-acid Change
NM_007294.4:c.5207T= MANE Select	NP_009225.1:p.Val1736=
ENST00000357654.9:c.5207T= MANE Select	ENSP00000350283.3:p.Val1736=
NM_007294.3:c.5207T= , LRG_292t1:c.5207T=	NP_009225.1:p.Val1736=
NM_007297.3:c.5066T=	NP_009228.2:p.Val1689=
NM_007297.4:c.5066T=	NP_009228.2:p.Val1689=
NM_007298.3:c.1895T=	NP_009229.2:p.Val632=
NM_007299.3:c.1895T=	NP_009230.2:p.Val632=
NM_007299.4:c.1895T=	NP_009230.2:p.Val632=
NM_007300.3:c.5270T=	NP_009231.2:p.Val1757=
NM_007300.4:c.5270T=	NP_009231.2:p.Val1757=
NR_027676.1:n.5343T=
NR_027676.2:n.5384T=
ENST00000352993.7:c.1781T=	ENSP00000312236.5:p.Val594=
ENST00000357654.7:c.5207T=	ENSP00000350283.3:p.Val1736=
ENST00000461221.5:c.*4990T=	ENSP00000418548.1:n.*4990T=
ENST00000461574.2:c.5204T=	ENSP00000417241.2:p.Val1735=
ENST00000468300.5:c.1895T=	ENSP00000417148.1:p.Val632=
ENST00000470026.6:c.5207T=	ENSP00000419274.2:p.Val1736=
ENST00000471181.6:c.5270T=	ENSP00000418960.2:p.Val1757=
ENST00000471181.7:c.5270T=	ENSP00000418960.2:p.Val1757=
ENST00000473961.6:c.5081T=	ENSP00000420201.2:p.Val1694=
ENST00000476777.6:c.5201T=	ENSP00000417554.2:p.Val1734=
ENST00000477152.6:c.5129T=	ENSP00000419988.2:p.Val1710=
ENST00000478531.6:c.1895T=	ENSP00000420412.2:p.Val632=
ENST00000484087.6:c.1769T=	ENSP00000419481.2:p.Val590=
ENST00000489037.2:c.5129T=	ENSP00000420781.2:p.Val1710=
ENST00000491747.6:c.1895T=	ENSP00000420705.2:p.Val632=
ENST00000493795.5:c.5066T=	ENSP00000418775.1:p.Val1689=
ENST00000493919.6:c.1757T=	ENSP00000418819.2:p.Val586=
ENST00000494123.6:c.5207T=	ENSP00000419103.2:p.Val1736=
ENST00000497488.2:c.4319T=	ENSP00000418986.2:p.Val1440=
ENST00000586385.5:c.137T=	ENSP00000465818.1:p.Val46=
ENST00000591534.5:c.680T=	ENSP00000467329.1:p.Val227=
ENST00000591849.5:c.-98-6932T=	ENSP00000465347.1:n.-98-6932T=
ENST00000618469.2:c.5207T=	ENSP00000478114.2:p.Val1736=
ENST00000634433.2:c.5084T=	ENSP00000489431.2:p.Val1695=
ENST00000644379.1:c.1594T=
ENST00000644379.2:c.5273T=	ENSP00000496570.2:p.Val1758=
ENST00000644555.2:c.1757T=	ENSP00000494614.2:p.Val586=
ENST00000652672.2:c.5066T=	ENSP00000498906.2:p.Val1689=