Canonical Allele Identifier: CA2260784334

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093785C= , CM000679.2:g.43093785C=	GRCh38
NC_000017.10:g.41245802C= , CM000679.1:g.41245802C=	GRCh37
NC_000017.9:g.38499328C=	NCBI36
NG_005905.2:g.124199G= , LRG_292:g.124199G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1810G=
ENST00000461574.2:c.1746G=	ENSP00000417241.2:p.Thr582=
ENST00000470026.6:c.1746G=	ENSP00000419274.2:p.Thr582=
ENST00000473961.6:c.1620G=	ENSP00000420201.2:p.Thr540=
ENST00000476777.6:c.1743G=	ENSP00000417554.2:p.Thr581=
ENST00000477152.6:c.1668G=	ENSP00000419988.2:p.Thr556=
ENST00000478531.6:c.784+959G=	ENSP00000420412.2:n.784+959G=
ENST00000489037.2:c.1668G=	ENSP00000420781.2:p.Thr556=
ENST00000493919.6:c.646+959G=	ENSP00000418819.2:n.646+959G=
ENST00000494123.6:c.1746G=	ENSP00000419103.2:p.Thr582=
ENST00000497488.2:c.858G=	ENSP00000418986.2:p.Thr286=
ENST00000618469.2:c.1746G=	ENSP00000478114.2:p.Thr582=
ENST00000634433.2:c.1623G=	ENSP00000489431.2:p.Thr541=
ENST00000644379.2:c.1746G=	ENSP00000496570.2:p.Thr582=
ENST00000644555.2:c.646+959G=	ENSP00000494614.2:n.646+959G=
ENST00000652672.2:c.1605G=	ENSP00000498906.2:p.Thr535=
ENST00000484087.6:c.664+959G=	ENSP00000419481.2:n.664+959G=
ENST00000700182.1:c.706+959G=	ENSP00000514849.1:n.706+959G=
ENST00000357654.9:c.1746G= MANE Select	ENSP00000350283.3:p.Thr582=
ENST00000471181.7:c.1746G=	ENSP00000418960.2:p.Thr582=
ENST00000652672.1:c.1605G=	ENSP00000498906.1:p.Thr535=
ENST00000352993.7:c.670+2061G=	ENSP00000312236.5:n.670+2061G=
ENST00000354071.7:c.1746G=	ENSP00000326002.7:p.Thr582=
ENST00000357654.7:c.1746G=	ENSP00000350283.3:p.Thr582=
ENST00000412061.3:c.1097G=
ENST00000461221.5:c.*1529G=	ENSP00000418548.1:n.*1529G=
ENST00000468300.5:c.787+959G=	ENSP00000417148.1:n.787+959G=
ENST00000470026.5:c.1746G=	ENSP00000419274.1:p.Thr582=
ENST00000471181.6:c.1746G=	ENSP00000418960.2:p.Thr582=
ENST00000477152.5:c.1668G=	ENSP00000419988.1:p.Thr556=
ENST00000478531.5:c.784+959G=	ENSP00000420412.1:n.784+959G=
ENST00000484087.5:c.409+959G=	ENSP00000419481.1:n.409+959G=
ENST00000487825.5:c.412+959G=	ENSP00000418212.1:n.412+959G=
ENST00000491747.6:c.787+959G=	ENSP00000420705.2:n.787+959G=
ENST00000493795.5:c.1605G=	ENSP00000418775.1:p.Thr535=
ENST00000493919.5:c.646+959G=	ENSP00000418819.1:n.646+959G=
ENST00000586385.5:c.5-29834G=	ENSP00000465818.1:n.5-29834G=
ENST00000591534.5:c.-43-19264G=	ENSP00000467329.1:n.-43-19264G=
ENST00000591849.5:c.-99+31486G=	ENSP00000465347.1:n.-99+31486G=
ENST00000634433.1:c.1623G=	ENSP00000489431.1:p.Thr541=
NM_007294.3:c.1746G= , LRG_292t1:c.1746G=	NP_009225.1:p.Thr582=
NM_007297.3:c.1605G=	NP_009228.2:p.Thr535=
NM_007298.3:c.787+959G=	NP_009229.2:n.787+959G=
NM_007299.3:c.787+959G=	NP_009230.2:n.787+959G=
NM_007300.3:c.1746G=	NP_009231.2:p.Thr582=
NR_027676.1:n.1882G=
NM_007294.4:c.1746G= MANE Select	NP_009225.1:p.Thr582=
NM_007297.4:c.1605G=	NP_009228.2:p.Thr535=
NM_007299.4:c.787+959G=	NP_009230.2:n.787+959G=
NM_007300.4:c.1746G=	NP_009231.2:p.Thr582=
NR_027676.2:n.1923G=