Canonical Allele Identifier: CA2260784837

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094334A= , CM000679.2:g.43094334A=	GRCh38
NC_000017.10:g.41246351A= , CM000679.1:g.41246351A=	GRCh37
NC_000017.9:g.38499877A=	NCBI36
NG_005905.2:g.123650T= , LRG_292:g.123650T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1261T=
ENST00000461574.2:c.1197T=	ENSP00000417241.2:p.His399=
ENST00000470026.6:c.1197T=	ENSP00000419274.2:p.His399=
ENST00000473961.6:c.1071T=	ENSP00000420201.2:p.His357=
ENST00000476777.6:c.1194T=	ENSP00000417554.2:p.His398=
ENST00000477152.6:c.1119T=	ENSP00000419988.2:p.His373=
ENST00000478531.6:c.784+410T=	ENSP00000420412.2:n.784+410T=
ENST00000489037.2:c.1119T=	ENSP00000420781.2:p.His373=
ENST00000493919.6:c.646+410T=	ENSP00000418819.2:n.646+410T=
ENST00000494123.6:c.1197T=	ENSP00000419103.2:p.His399=
ENST00000497488.2:c.309T=	ENSP00000418986.2:p.His103=
ENST00000618469.2:c.1197T=	ENSP00000478114.2:p.His399=
ENST00000634433.2:c.1074T=	ENSP00000489431.2:p.His358=
ENST00000644379.2:c.1197T=	ENSP00000496570.2:p.His399=
ENST00000644555.2:c.646+410T=	ENSP00000494614.2:n.646+410T=
ENST00000652672.2:c.1056T=	ENSP00000498906.2:p.His352=
ENST00000484087.6:c.664+410T=	ENSP00000419481.2:n.664+410T=
ENST00000700182.1:c.706+410T=	ENSP00000514849.1:n.706+410T=
ENST00000700183.1:c.*1205T=	ENSP00000514850.1:n.*1205T=
ENST00000357654.9:c.1197T= MANE Select	ENSP00000350283.3:p.His399=
ENST00000471181.7:c.1197T=	ENSP00000418960.2:p.His399=
ENST00000652672.1:c.1056T=	ENSP00000498906.1:p.His352=
ENST00000352993.7:c.670+1512T=	ENSP00000312236.5:n.670+1512T=
ENST00000354071.7:c.1197T=	ENSP00000326002.7:p.His399=
ENST00000357654.7:c.1197T=	ENSP00000350283.3:p.His399=
ENST00000412061.3:c.548T=
ENST00000461221.5:c.*980T=	ENSP00000418548.1:n.*980T=
ENST00000468300.5:c.787+410T=	ENSP00000417148.1:n.787+410T=
ENST00000470026.5:c.1197T=	ENSP00000419274.1:p.His399=
ENST00000471181.6:c.1197T=	ENSP00000418960.2:p.His399=
ENST00000473961.5:c.794T=
ENST00000477152.5:c.1119T=	ENSP00000419988.1:p.His373=
ENST00000478531.5:c.784+410T=	ENSP00000420412.1:n.784+410T=
ENST00000484087.5:c.409+410T=	ENSP00000419481.1:n.409+410T=
ENST00000487825.5:c.412+410T=	ENSP00000418212.1:n.412+410T=
ENST00000491747.6:c.787+410T=	ENSP00000420705.2:n.787+410T=
ENST00000492859.5:c.*1133T=	ENSP00000420253.1:n.*1133T=
ENST00000493795.5:c.1056T=	ENSP00000418775.1:p.His352=
ENST00000493919.5:c.646+410T=	ENSP00000418819.1:n.646+410T=
ENST00000494123.5:c.1197T=	ENSP00000419103.1:p.His399=
ENST00000497488.1:c.309T=	ENSP00000418986.1:p.His103=
ENST00000586385.5:c.5-30383T=	ENSP00000465818.1:n.5-30383T=
ENST00000591534.5:c.-43-19813T=	ENSP00000467329.1:n.-43-19813T=
ENST00000591849.5:c.-99+30937T=	ENSP00000465347.1:n.-99+30937T=
ENST00000634433.1:c.1074T=	ENSP00000489431.1:p.His358=
NM_007294.3:c.1197T= , LRG_292t1:c.1197T=	NP_009225.1:p.His399=
NM_007297.3:c.1056T=	NP_009228.2:p.His352=
NM_007298.3:c.787+410T=	NP_009229.2:n.787+410T=
NM_007299.3:c.787+410T=	NP_009230.2:n.787+410T=
NM_007300.3:c.1197T=	NP_009231.2:p.His399=
NR_027676.1:n.1333T=
NM_007294.4:c.1197T= MANE Select	NP_009225.1:p.His399=
NM_007297.4:c.1056T=	NP_009228.2:p.His352=
NM_007299.4:c.787+410T=	NP_009230.2:n.787+410T=
NM_007300.4:c.1197T=	NP_009231.2:p.His399=
NR_027676.2:n.1374T=