Canonical Allele Identifier: CA2260774442

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43074354G= , CM000679.2:g.43074354G=	GRCh38
NC_000017.10:g.41226371G= , CM000679.1:g.41226371G=	GRCh37
NC_000017.9:g.38479897G=	NCBI36
NG_005905.2:g.143630C= , LRG_292:g.143630C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000461574.2:c.4649C=	ENSP00000417241.2:p.Ser1550=
ENST00000470026.6:c.4652C=	ENSP00000419274.2:p.Ser1551=
ENST00000473961.6:c.4526C=	ENSP00000420201.2:p.Ser1509=
ENST00000476777.6:c.4646C=	ENSP00000417554.2:p.Ser1549=
ENST00000477152.6:c.4574C=	ENSP00000419988.2:p.Ser1525=
ENST00000478531.6:c.1340C=	ENSP00000420412.2:p.Ser447=
ENST00000489037.2:c.4574C=	ENSP00000420781.2:p.Ser1525=
ENST00000493919.6:c.1202C=	ENSP00000418819.2:p.Ser401=
ENST00000494123.6:c.4652C=	ENSP00000419103.2:p.Ser1551=
ENST00000497488.2:c.3764C=	ENSP00000418986.2:p.Ser1255=
ENST00000618469.2:c.4652C=	ENSP00000478114.2:p.Ser1551=
ENST00000634433.2:c.4529C=	ENSP00000489431.2:p.Ser1510=
ENST00000644379.2:c.4718C=	ENSP00000496570.2:p.Ser1573=
ENST00000644555.2:c.1202C=	ENSP00000494614.2:p.Ser401=
ENST00000652672.2:c.4511C=	ENSP00000498906.2:p.Ser1504=
ENST00000484087.6:c.1214C=	ENSP00000419481.2:p.Ser405=
ENST00000700182.1:c.1259C=	ENSP00000514849.1:p.Ser420=
ENST00000357654.9:c.4652C= MANE Select	ENSP00000350283.3:p.Ser1551=
ENST00000471181.7:c.4715C=	ENSP00000418960.2:p.Ser1572=
ENST00000644379.1:c.1039C=
ENST00000352993.7:c.1226C=	ENSP00000312236.5:p.Ser409=
ENST00000357654.7:c.4652C=	ENSP00000350283.3:p.Ser1551=
ENST00000461221.5:c.*4435C=	ENSP00000418548.1:n.*4435C=
ENST00000468300.5:c.1340C=	ENSP00000417148.1:p.Ser447=
ENST00000471181.6:c.4715C=	ENSP00000418960.2:p.Ser1572=
ENST00000478531.5:c.1340C=	ENSP00000420412.1:p.Ser447=
ENST00000484087.5:c.965C=	ENSP00000419481.1:p.Ser322=
ENST00000491747.6:c.1340C=	ENSP00000420705.2:p.Ser447=
ENST00000493795.5:c.4511C=	ENSP00000418775.1:p.Ser1504=
ENST00000493919.5:c.1202C=	ENSP00000418819.1:p.Ser401=
ENST00000586385.5:c.5-10403C=	ENSP00000465818.1:n.5-10403C=
ENST00000591534.5:c.125C=	ENSP00000467329.1:p.Ser42=
ENST00000591849.5:c.-98-24164C=	ENSP00000465347.1:n.-98-24164C=
NM_007294.3:c.4652C= , LRG_292t1:c.4652C=	NP_009225.1:p.Ser1551=
NM_007297.3:c.4511C=	NP_009228.2:p.Ser1504=
NM_007298.3:c.1340C=	NP_009229.2:p.Ser447=
NM_007299.3:c.1340C=	NP_009230.2:p.Ser447=
NM_007300.3:c.4715C=	NP_009231.2:p.Ser1572=
NR_027676.1:n.4788C=
NM_007294.4:c.4652C= MANE Select	NP_009225.1:p.Ser1551=
NM_007297.4:c.4511C=	NP_009228.2:p.Ser1504=
NM_007299.4:c.1340C=	NP_009230.2:p.Ser447=
NM_007300.4:c.4715C=	NP_009231.2:p.Ser1572=
NR_027676.2:n.4829C=