Canonical Allele Identifier: CA2260771338

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067633C= , CM000679.2:g.43067633C=	GRCh38
NC_000017.10:g.41219650C= , CM000679.1:g.41219650C=	GRCh37
NC_000017.9:g.38473176C=	NCBI36
NG_005905.2:g.150351G= , LRG_292:g.150351G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.5046G=	ENSP00000417241.2:p.Glu1682=
ENST00000470026.6:c.5049G=	ENSP00000419274.2:p.Glu1683=
ENST00000473961.6:c.4923G=	ENSP00000420201.2:p.Glu1641=
ENST00000476777.6:c.5043G=	ENSP00000417554.2:p.Glu1681=
ENST00000477152.6:c.4971G=	ENSP00000419988.2:p.Glu1657=
ENST00000478531.6:c.1737G=	ENSP00000420412.2:p.Glu579=
ENST00000489037.2:c.4971G=	ENSP00000420781.2:p.Glu1657=
ENST00000493919.6:c.1599G=	ENSP00000418819.2:p.Glu533=
ENST00000494123.6:c.5049G=	ENSP00000419103.2:p.Glu1683=
ENST00000497488.2:c.4161G=	ENSP00000418986.2:p.Glu1387=
ENST00000618469.2:c.5049G=	ENSP00000478114.2:p.Glu1683=
ENST00000634433.2:c.4926G=	ENSP00000489431.2:p.Glu1642=
ENST00000644379.2:c.5115G=	ENSP00000496570.2:p.Glu1705=
ENST00000644555.2:c.1599G=	ENSP00000494614.2:p.Glu533=
ENST00000652672.2:c.4908G=	ENSP00000498906.2:p.Glu1636=
ENST00000484087.6:c.1611G=	ENSP00000419481.2:p.Glu537=
ENST00000357654.9:c.5049G= MANE Select	ENSP00000350283.3:p.Glu1683=
ENST00000471181.7:c.5112G=	ENSP00000418960.2:p.Glu1704=
ENST00000644379.1:c.1436G=
ENST00000352993.7:c.1623G=	ENSP00000312236.5:p.Glu541=
ENST00000357654.7:c.5049G=	ENSP00000350283.3:p.Glu1683=
ENST00000461221.5:c.*4832G=	ENSP00000418548.1:n.*4832G=
ENST00000468300.5:c.1737G=	ENSP00000417148.1:p.Glu579=
ENST00000471181.6:c.5112G=	ENSP00000418960.2:p.Glu1704=
ENST00000472490.1:n.202G=
ENST00000478531.5:c.1737G=	ENSP00000420412.1:p.Glu579=
ENST00000484087.5:c.1362G=	ENSP00000419481.1:p.Glu454=
ENST00000491747.6:c.1737G=	ENSP00000420705.2:p.Glu579=
ENST00000493795.5:c.4908G=	ENSP00000418775.1:p.Glu1636=
ENST00000493919.5:c.1599G=	ENSP00000418819.1:p.Glu533=
ENST00000586385.5:c.5-3682G=	ENSP00000465818.1:n.5-3682G=
ENST00000591534.5:c.522G=	ENSP00000467329.1:p.Glu174=
ENST00000591849.5:c.-98-17443G=	ENSP00000465347.1:n.-98-17443G=
NM_007294.3:c.5049G= , LRG_292t1:c.5049G=	NP_009225.1:p.Glu1683=
NM_007297.3:c.4908G=	NP_009228.2:p.Glu1636=
NM_007298.3:c.1737G=	NP_009229.2:p.Glu579=
NM_007299.3:c.1737G=	NP_009230.2:p.Glu579=
NM_007300.3:c.5112G=	NP_009231.2:p.Glu1704=
NR_027676.1:n.5185G=
NM_007294.4:c.5049G= MANE Select	NP_009225.1:p.Glu1683=
NM_007297.4:c.4908G=	NP_009228.2:p.Glu1636=
NM_007299.4:c.1737G=	NP_009230.2:p.Glu579=
NM_007300.4:c.5112G=	NP_009231.2:p.Glu1704=
NR_027676.2:n.5226G=