Canonical Allele Identifier: CA2260775492

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43076549C= , CM000679.2:g.43076549C=	GRCh38
NC_000017.10:g.41228566C= , CM000679.1:g.41228566C=	GRCh37
NC_000017.9:g.38482092C=	NCBI36
NG_005905.2:g.141435G= , LRG_292:g.141435G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4420G=	ENSP00000417241.2:p.Asp1474=
ENST00000470026.6:c.4423G=	ENSP00000419274.2:p.Asp1475=
ENST00000473961.6:c.4297G=	ENSP00000420201.2:p.Asp1433=
ENST00000476777.6:c.4417G=	ENSP00000417554.2:p.Asp1473=
ENST00000477152.6:c.4345G=	ENSP00000419988.2:p.Asp1449=
ENST00000478531.6:c.1111G=	ENSP00000420412.2:p.Asp371=
ENST00000489037.2:c.4345G=	ENSP00000420781.2:p.Asp1449=
ENST00000493919.6:c.973G=	ENSP00000418819.2:p.Asp325=
ENST00000494123.6:c.4423G=	ENSP00000419103.2:p.Asp1475=
ENST00000497488.2:c.3535G=	ENSP00000418986.2:p.Asp1179=
ENST00000618469.2:c.4423G=	ENSP00000478114.2:p.Asp1475=
ENST00000634433.2:c.4300G=	ENSP00000489431.2:p.Asp1434=
ENST00000644379.2:c.4489G=	ENSP00000496570.2:p.Asp1497=
ENST00000644555.2:c.973G=	ENSP00000494614.2:p.Asp325=
ENST00000652672.2:c.4282G=	ENSP00000498906.2:p.Asp1428=
ENST00000484087.6:c.985G=	ENSP00000419481.2:p.Asp329=
ENST00000700182.1:c.1030G=	ENSP00000514849.1:p.Asp344=
ENST00000357654.9:c.4423G= MANE Select	ENSP00000350283.3:p.Asp1475=
ENST00000471181.7:c.4486G=	ENSP00000418960.2:p.Asp1496=
ENST00000644379.1:c.810G=
ENST00000352993.7:c.997G=	ENSP00000312236.5:p.Asp333=
ENST00000357654.7:c.4423G=	ENSP00000350283.3:p.Asp1475=
ENST00000461221.5:c.*4206G=	ENSP00000418548.1:n.*4206G=
ENST00000461574.1:c.714G=
ENST00000468300.5:c.1111G=	ENSP00000417148.1:p.Asp371=
ENST00000471181.6:c.4486G=	ENSP00000418960.2:p.Asp1496=
ENST00000478531.5:c.1111G=	ENSP00000420412.1:p.Asp371=
ENST00000484087.5:c.736G=	ENSP00000419481.1:p.Asp246=
ENST00000487825.5:c.739G=	ENSP00000418212.1:p.Asp247=
ENST00000491747.6:c.1111G=	ENSP00000420705.2:p.Asp371=
ENST00000493795.5:c.4282G=	ENSP00000418775.1:p.Asp1428=
ENST00000493919.5:c.973G=	ENSP00000418819.1:p.Asp325=
ENST00000586385.5:c.5-12598G=	ENSP00000465818.1:n.5-12598G=
ENST00000591534.5:c.-43-2028G=	ENSP00000467329.1:n.-43-2028G=
ENST00000591849.5:c.-98-26359G=	ENSP00000465347.1:n.-98-26359G=
ENST00000621897.1:n.314G=
NM_007294.3:c.4423G= , LRG_292t1:c.4423G=	NP_009225.1:p.Asp1475=
NM_007297.3:c.4282G=	NP_009228.2:p.Asp1428=
NM_007298.3:c.1111G=	NP_009229.2:p.Asp371=
NM_007299.3:c.1111G=	NP_009230.2:p.Asp371=
NM_007300.3:c.4486G=	NP_009231.2:p.Asp1496=
NR_027676.1:n.4559G=
NM_007294.4:c.4423G= MANE Select	NP_009225.1:p.Asp1475=
NM_007297.4:c.4282G=	NP_009228.2:p.Asp1428=
NM_007299.4:c.1111G=	NP_009230.2:p.Asp371=
NM_007300.4:c.4486G=	NP_009231.2:p.Asp1496=
NR_027676.2:n.4600G=