Canonical Allele Identifier: CA2260771408

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43067689C= , CM000679.2:g.43067689C=	GRCh38
NC_000017.10:g.41219706C= , CM000679.1:g.41219706C=	GRCh37
NC_000017.9:g.38473232C=	NCBI36
NG_005905.2:g.150295G= , LRG_292:g.150295G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4990G=	ENSP00000417241.2:p.Val1664=
ENST00000470026.6:c.4993G=	ENSP00000419274.2:p.Val1665=
ENST00000473961.6:c.4867G=	ENSP00000420201.2:p.Val1623=
ENST00000476777.6:c.4987G=	ENSP00000417554.2:p.Val1663=
ENST00000477152.6:c.4915G=	ENSP00000419988.2:p.Val1639=
ENST00000478531.6:c.1681G=	ENSP00000420412.2:p.Val561=
ENST00000489037.2:c.4915G=	ENSP00000420781.2:p.Val1639=
ENST00000493919.6:c.1543G=	ENSP00000418819.2:p.Val515=
ENST00000494123.6:c.4993G=	ENSP00000419103.2:p.Val1665=
ENST00000497488.2:c.4105G=	ENSP00000418986.2:p.Val1369=
ENST00000618469.2:c.4993G=	ENSP00000478114.2:p.Val1665=
ENST00000634433.2:c.4870G=	ENSP00000489431.2:p.Val1624=
ENST00000644379.2:c.5059G=	ENSP00000496570.2:p.Val1687=
ENST00000644555.2:c.1543G=	ENSP00000494614.2:p.Val515=
ENST00000652672.2:c.4852G=	ENSP00000498906.2:p.Val1618=
ENST00000484087.6:c.1555G=	ENSP00000419481.2:p.Val519=
ENST00000357654.9:c.4993G= MANE Select	ENSP00000350283.3:p.Val1665=
ENST00000471181.7:c.5056G=	ENSP00000418960.2:p.Val1686=
ENST00000644379.1:c.1380G=
ENST00000352993.7:c.1567G=	ENSP00000312236.5:p.Val523=
ENST00000357654.7:c.4993G=	ENSP00000350283.3:p.Val1665=
ENST00000461221.5:c.*4776G=	ENSP00000418548.1:n.*4776G=
ENST00000468300.5:c.1681G=	ENSP00000417148.1:p.Val561=
ENST00000471181.6:c.5056G=	ENSP00000418960.2:p.Val1686=
ENST00000472490.1:n.146G=
ENST00000478531.5:c.1681G=	ENSP00000420412.1:p.Val561=
ENST00000484087.5:c.1306G=	ENSP00000419481.1:p.Val436=
ENST00000491747.6:c.1681G=	ENSP00000420705.2:p.Val561=
ENST00000493795.5:c.4852G=	ENSP00000418775.1:p.Val1618=
ENST00000493919.5:c.1543G=	ENSP00000418819.1:p.Val515=
ENST00000586385.5:c.5-3738G=	ENSP00000465818.1:n.5-3738G=
ENST00000591534.5:c.466G=	ENSP00000467329.1:p.Val156=
ENST00000591849.5:c.-98-17499G=	ENSP00000465347.1:n.-98-17499G=
NM_007294.3:c.4993G= , LRG_292t1:c.4993G=	NP_009225.1:p.Val1665=
NM_007297.3:c.4852G=	NP_009228.2:p.Val1618=
NM_007298.3:c.1681G=	NP_009229.2:p.Val561=
NM_007299.3:c.1681G=	NP_009230.2:p.Val561=
NM_007300.3:c.5056G=	NP_009231.2:p.Val1686=
NR_027676.1:n.5129G=
NM_007294.4:c.4993G= MANE Select	NP_009225.1:p.Val1665=
NM_007297.4:c.4852G=	NP_009228.2:p.Val1618=
NM_007299.4:c.1681G=	NP_009230.2:p.Val561=
NM_007300.4:c.5056G=	NP_009231.2:p.Val1686=
NR_027676.2:n.5170G=