Canonical Allele Identifier: CA2260771410

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067691A= , CM000679.2:g.43067691A=	GRCh38
NC_000017.10:g.41219708A= , CM000679.1:g.41219708A=	GRCh37
NC_000017.9:g.38473234A=	NCBI36
NG_005905.2:g.150293T= , LRG_292:g.150293T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4988T=	ENSP00000417241.2:p.Leu1663=
ENST00000470026.6:c.4991T=	ENSP00000419274.2:p.Leu1664=
ENST00000473961.6:c.4865T=	ENSP00000420201.2:p.Leu1622=
ENST00000476777.6:c.4985T=	ENSP00000417554.2:p.Leu1662=
ENST00000477152.6:c.4913T=	ENSP00000419988.2:p.Leu1638=
ENST00000478531.6:c.1679T=	ENSP00000420412.2:p.Leu560=
ENST00000489037.2:c.4913T=	ENSP00000420781.2:p.Leu1638=
ENST00000493919.6:c.1541T=	ENSP00000418819.2:p.Leu514=
ENST00000494123.6:c.4991T=	ENSP00000419103.2:p.Leu1664=
ENST00000497488.2:c.4103T=	ENSP00000418986.2:p.Leu1368=
ENST00000618469.2:c.4991T=	ENSP00000478114.2:p.Leu1664=
ENST00000634433.2:c.4868T=	ENSP00000489431.2:p.Leu1623=
ENST00000644379.2:c.5057T=	ENSP00000496570.2:p.Leu1686=
ENST00000644555.2:c.1541T=	ENSP00000494614.2:p.Leu514=
ENST00000652672.2:c.4850T=	ENSP00000498906.2:p.Leu1617=
ENST00000484087.6:c.1553T=	ENSP00000419481.2:p.Leu518=
ENST00000357654.9:c.4991T= MANE Select	ENSP00000350283.3:p.Leu1664=
ENST00000471181.7:c.5054T=	ENSP00000418960.2:p.Leu1685=
ENST00000644379.1:c.1378T=
ENST00000352993.7:c.1565T=	ENSP00000312236.5:p.Leu522=
ENST00000357654.7:c.4991T=	ENSP00000350283.3:p.Leu1664=
ENST00000461221.5:c.*4774T=	ENSP00000418548.1:n.*4774T=
ENST00000468300.5:c.1679T=	ENSP00000417148.1:p.Leu560=
ENST00000471181.6:c.5054T=	ENSP00000418960.2:p.Leu1685=
ENST00000472490.1:n.144T=
ENST00000478531.5:c.1679T=	ENSP00000420412.1:p.Leu560=
ENST00000484087.5:c.1304T=	ENSP00000419481.1:p.Leu435=
ENST00000491747.6:c.1679T=	ENSP00000420705.2:p.Leu560=
ENST00000493795.5:c.4850T=	ENSP00000418775.1:p.Leu1617=
ENST00000493919.5:c.1541T=	ENSP00000418819.1:p.Leu514=
ENST00000586385.5:c.5-3740T=	ENSP00000465818.1:n.5-3740T=
ENST00000591534.5:c.464T=	ENSP00000467329.1:p.Leu155=
ENST00000591849.5:c.-98-17501T=	ENSP00000465347.1:n.-98-17501T=
NM_007294.3:c.4991T= , LRG_292t1:c.4991T=	NP_009225.1:p.Leu1664=
NM_007297.3:c.4850T=	NP_009228.2:p.Leu1617=
NM_007298.3:c.1679T=	NP_009229.2:p.Leu560=
NM_007299.3:c.1679T=	NP_009230.2:p.Leu560=
NM_007300.3:c.5054T=	NP_009231.2:p.Leu1685=
NR_027676.1:n.5127T=
NM_007294.4:c.4991T= MANE Select	NP_009225.1:p.Leu1664=
NM_007297.4:c.4850T=	NP_009228.2:p.Leu1617=
NM_007299.4:c.1679T=	NP_009230.2:p.Leu560=
NM_007300.4:c.5054T=	NP_009231.2:p.Leu1685=
NR_027676.2:n.5168T=