Canonical Allele Identifier: CA2260772887

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43071072T= , CM000679.2:g.43071072T=	GRCh38
NC_000017.10:g.41223089T= , CM000679.1:g.41223089T=	GRCh37
NC_000017.9:g.38476615T=	NCBI36
NG_005905.2:g.146912A= , LRG_292:g.146912A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4839A=	ENSP00000417241.2:p.Pro1613=
ENST00000470026.6:c.4842A=	ENSP00000419274.2:p.Pro1614=
ENST00000473961.6:c.4716A=	ENSP00000420201.2:p.Pro1572=
ENST00000476777.6:c.4836A=	ENSP00000417554.2:p.Pro1612=
ENST00000477152.6:c.4764A=	ENSP00000419988.2:p.Pro1588=
ENST00000478531.6:c.1530A=	ENSP00000420412.2:p.Pro510=
ENST00000489037.2:c.4764A=	ENSP00000420781.2:p.Pro1588=
ENST00000493919.6:c.1392A=	ENSP00000418819.2:p.Pro464=
ENST00000494123.6:c.4842A=	ENSP00000419103.2:p.Pro1614=
ENST00000497488.2:c.3954A=	ENSP00000418986.2:p.Pro1318=
ENST00000618469.2:c.4842A=	ENSP00000478114.2:p.Pro1614=
ENST00000634433.2:c.4719A=	ENSP00000489431.2:p.Pro1573=
ENST00000644379.2:c.4908A=	ENSP00000496570.2:p.Pro1636=
ENST00000644555.2:c.1392A=	ENSP00000494614.2:p.Pro464=
ENST00000652672.2:c.4701A=	ENSP00000498906.2:p.Pro1567=
ENST00000484087.6:c.1404A=	ENSP00000419481.2:p.Pro468=
ENST00000700182.1:c.1449A=	ENSP00000514849.1:p.Pro483=
ENST00000357654.9:c.4842A= MANE Select	ENSP00000350283.3:p.Pro1614=
ENST00000471181.7:c.4905A=	ENSP00000418960.2:p.Pro1635=
ENST00000644379.1:c.1229A=
ENST00000352993.7:c.1416A=	ENSP00000312236.5:p.Pro472=
ENST00000357654.7:c.4842A=	ENSP00000350283.3:p.Pro1614=
ENST00000461221.5:c.*4625A=	ENSP00000418548.1:n.*4625A=
ENST00000468300.5:c.1530A=	ENSP00000417148.1:p.Pro510=
ENST00000471181.6:c.4905A=	ENSP00000418960.2:p.Pro1635=
ENST00000478531.5:c.1530A=	ENSP00000420412.1:p.Pro510=
ENST00000484087.5:c.1155A=	ENSP00000419481.1:p.Pro385=
ENST00000491747.6:c.1530A=	ENSP00000420705.2:p.Pro510=
ENST00000493795.5:c.4701A=	ENSP00000418775.1:p.Pro1567=
ENST00000493919.5:c.1392A=	ENSP00000418819.1:p.Pro464=
ENST00000586385.5:c.5-7121A=	ENSP00000465818.1:n.5-7121A=
ENST00000591534.5:c.315A=	ENSP00000467329.1:p.Pro105=
ENST00000591849.5:c.-98-20882A=	ENSP00000465347.1:n.-98-20882A=
NM_007294.3:c.4842A= , LRG_292t1:c.4842A=	NP_009225.1:p.Pro1614=
NM_007297.3:c.4701A=	NP_009228.2:p.Pro1567=
NM_007298.3:c.1530A=	NP_009229.2:p.Pro510=
NM_007299.3:c.1530A=	NP_009230.2:p.Pro510=
NM_007300.3:c.4905A=	NP_009231.2:p.Pro1635=
NR_027676.1:n.4978A=
NM_007294.4:c.4842A= MANE Select	NP_009225.1:p.Pro1614=
NM_007297.4:c.4701A=	NP_009228.2:p.Pro1567=
NM_007299.4:c.1530A=	NP_009230.2:p.Pro510=
NM_007300.4:c.4905A=	NP_009231.2:p.Pro1635=
NR_027676.2:n.5019A=