Canonical Allele Identifier: CA2260761131

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43045777A= , CM000679.2:g.43045777A=	GRCh38
NC_000017.10:g.41197794A= , CM000679.1:g.41197794A=	GRCh37
NC_000017.9:g.38451320A=	NCBI36
NG_005905.2:g.172207T= , LRG_292:g.172207T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5490T=	ENSP00000417241.2:p.Pro1830=
ENST00000470026.6:c.5493T=	ENSP00000419274.2:p.Pro1831=
ENST00000473961.6:c.5367T=	ENSP00000420201.2:p.Pro1789=
ENST00000476777.6:c.5487T=	ENSP00000417554.2:p.Pro1829=
ENST00000477152.6:c.5415T=	ENSP00000419988.2:p.Pro1805=
ENST00000478531.6:c.2181T=	ENSP00000420412.2:p.Pro727=
ENST00000489037.2:c.5415T=	ENSP00000420781.2:p.Pro1805=
ENST00000493919.6:c.2043T=	ENSP00000418819.2:p.Pro681=
ENST00000494123.6:c.5493T=	ENSP00000419103.2:p.Pro1831=
ENST00000497488.2:c.4605T=	ENSP00000418986.2:p.Pro1535=
ENST00000618469.2:c.5493T=	ENSP00000478114.2:p.Pro1831=
ENST00000634433.2:c.5370T=	ENSP00000489431.2:p.Pro1790=
ENST00000644379.2:c.5559T=	ENSP00000496570.2:p.Pro1853=
ENST00000644555.2:c.2043T=	ENSP00000494614.2:p.Pro681=
ENST00000652672.2:c.5352T=	ENSP00000498906.2:p.Pro1784=
ENST00000484087.6:c.2055T=	ENSP00000419481.2:p.Pro685=
ENST00000700081.1:n.1376T=
ENST00000700082.1:n.857T=
ENST00000357654.9:c.5493T= MANE Select	ENSP00000350283.3:p.Pro1831=
ENST00000471181.7:c.5556T=	ENSP00000418960.2:p.Pro1852=
ENST00000644379.1:c.1880T=
ENST00000352993.7:c.2067T=	ENSP00000312236.5:p.Pro689=
ENST00000357654.7:c.5493T=	ENSP00000350283.3:p.Pro1831=
ENST00000461221.5:c.*5276T=	ENSP00000418548.1:n.*5276T=
ENST00000468300.5:c.*7T=	ENSP00000417148.1:n.*7T=
ENST00000471181.6:c.5556T=	ENSP00000418960.2:p.Pro1852=
ENST00000491747.6:c.2181T=	ENSP00000420705.2:p.Pro727=
ENST00000493795.5:c.5352T=	ENSP00000418775.1:p.Pro1784=
ENST00000586385.5:c.423T=	ENSP00000465818.1:p.Pro141=
ENST00000591534.5:c.966T=	ENSP00000467329.1:p.Pro322=
ENST00000591849.5:c.192T=	ENSP00000465347.1:p.Pro64=
NM_007294.3:c.5493T= , LRG_292t1:c.5493T=	NP_009225.1:p.Pro1831=
NM_007297.3:c.5352T=	NP_009228.2:p.Pro1784=
NM_007298.3:c.2181T=	NP_009229.2:p.Pro727=
NM_007299.3:c.*7T=	NP_009230.2:n.*7T=
NM_007300.3:c.5556T=	NP_009231.2:p.Pro1852=
NR_027676.1:n.5629T=
NM_007294.4:c.5493T= MANE Select	NP_009225.1:p.Pro1831=
NM_007297.4:c.5352T=	NP_009228.2:p.Pro1784=
NM_007299.4:c.*7T=	NP_009230.2:n.*7T=
NM_007300.4:c.5556T=	NP_009231.2:p.Pro1852=
NR_027676.2:n.5670T=