Canonical Allele Identifier: CA2260772955

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43071143C= , CM000679.2:g.43071143C=	GRCh38
NC_000017.10:g.41223160C= , CM000679.1:g.41223160C=	GRCh37
NC_000017.9:g.38476686C=	NCBI36
NG_005905.2:g.146841G= , LRG_292:g.146841G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4768G=	ENSP00000417241.2:p.Gly1590=
ENST00000470026.6:c.4771G=	ENSP00000419274.2:p.Gly1591=
ENST00000473961.6:c.4645G=	ENSP00000420201.2:p.Gly1549=
ENST00000476777.6:c.4765G=	ENSP00000417554.2:p.Gly1589=
ENST00000477152.6:c.4693G=	ENSP00000419988.2:p.Gly1565=
ENST00000478531.6:c.1459G=	ENSP00000420412.2:p.Gly487=
ENST00000489037.2:c.4693G=	ENSP00000420781.2:p.Gly1565=
ENST00000493919.6:c.1321G=	ENSP00000418819.2:p.Gly441=
ENST00000494123.6:c.4771G=	ENSP00000419103.2:p.Gly1591=
ENST00000497488.2:c.3883G=	ENSP00000418986.2:p.Gly1295=
ENST00000618469.2:c.4771G=	ENSP00000478114.2:p.Gly1591=
ENST00000634433.2:c.4648G=	ENSP00000489431.2:p.Gly1550=
ENST00000644379.2:c.4837G=	ENSP00000496570.2:p.Gly1613=
ENST00000644555.2:c.1321G=	ENSP00000494614.2:p.Gly441=
ENST00000652672.2:c.4630G=	ENSP00000498906.2:p.Gly1544=
ENST00000484087.6:c.1333G=	ENSP00000419481.2:p.Gly445=
ENST00000700182.1:c.1378G=	ENSP00000514849.1:p.Gly460=
ENST00000357654.9:c.4771G= MANE Select	ENSP00000350283.3:p.Gly1591=
ENST00000471181.7:c.4834G=	ENSP00000418960.2:p.Gly1612=
ENST00000644379.1:c.1158G=
ENST00000352993.7:c.1345G=	ENSP00000312236.5:p.Gly449=
ENST00000357654.7:c.4771G=	ENSP00000350283.3:p.Gly1591=
ENST00000461221.5:c.*4554G=	ENSP00000418548.1:n.*4554G=
ENST00000468300.5:c.1459G=	ENSP00000417148.1:p.Gly487=
ENST00000471181.6:c.4834G=	ENSP00000418960.2:p.Gly1612=
ENST00000478531.5:c.1459G=	ENSP00000420412.1:p.Gly487=
ENST00000484087.5:c.1084G=	ENSP00000419481.1:p.Gly362=
ENST00000491747.6:c.1459G=	ENSP00000420705.2:p.Gly487=
ENST00000493795.5:c.4630G=	ENSP00000418775.1:p.Gly1544=
ENST00000493919.5:c.1321G=	ENSP00000418819.1:p.Gly441=
ENST00000586385.5:c.5-7192G=	ENSP00000465818.1:n.5-7192G=
ENST00000591534.5:c.244G=	ENSP00000467329.1:p.Gly82=
ENST00000591849.5:c.-98-20953G=	ENSP00000465347.1:n.-98-20953G=
NM_007294.3:c.4771G= , LRG_292t1:c.4771G=	NP_009225.1:p.Gly1591=
NM_007297.3:c.4630G=	NP_009228.2:p.Gly1544=
NM_007298.3:c.1459G=	NP_009229.2:p.Gly487=
NM_007299.3:c.1459G=	NP_009230.2:p.Gly487=
NM_007300.3:c.4834G=	NP_009231.2:p.Gly1612=
NR_027676.1:n.4907G=
NM_007294.4:c.4771G= MANE Select	NP_009225.1:p.Gly1591=
NM_007297.4:c.4630G=	NP_009228.2:p.Gly1544=
NM_007299.4:c.1459G=	NP_009230.2:p.Gly487=
NM_007300.4:c.4834G=	NP_009231.2:p.Gly1612=
NR_027676.2:n.4948G=