Canonical Allele Identifier: CA2260784870
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094383T= , CM000679.2:g.43094383T= GRCh38
NC_000017.10:g.41246400T= , CM000679.1:g.41246400T= GRCh37
NC_000017.9:g.38499926T= NCBI36
NG_005905.2:g.123601A= , LRG_292:g.123601A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.1212A=
ENST00000461574.2:c.1148A= ENSP00000417241.2:p.Asn383=
ENST00000470026.6:c.1148A= ENSP00000419274.2:p.Asn383=
ENST00000473961.6:c.1022A= ENSP00000420201.2:p.Asn341=
ENST00000476777.6:c.1145A= ENSP00000417554.2:p.Asn382=
ENST00000477152.6:c.1070A= ENSP00000419988.2:p.Asn357=
ENST00000478531.6:c.784+361A= ENSP00000420412.2:n.784+361A=
ENST00000489037.2:c.1070A= ENSP00000420781.2:p.Asn357=
ENST00000493919.6:c.646+361A= ENSP00000418819.2:n.646+361A=
ENST00000494123.6:c.1148A= ENSP00000419103.2:p.Asn383=
ENST00000497488.2:c.260A= ENSP00000418986.2:p.Asn87=
ENST00000618469.2:c.1148A= ENSP00000478114.2:p.Asn383=
ENST00000634433.2:c.1025A= ENSP00000489431.2:p.Asn342=
ENST00000644379.2:c.1148A= ENSP00000496570.2:p.Asn383=
ENST00000644555.2:c.646+361A= ENSP00000494614.2:n.646+361A=
ENST00000652672.2:c.1007A= ENSP00000498906.2:p.Asn336=
ENST00000484087.6:c.664+361A= ENSP00000419481.2:n.664+361A=
ENST00000700182.1:c.706+361A= ENSP00000514849.1:n.706+361A=
ENST00000700183.1:c.*1156A= ENSP00000514850.1:n.*1156A=
ENST00000357654.9:c.1148A= MANE Select ENSP00000350283.3:p.Asn383=
ENST00000471181.7:c.1148A= ENSP00000418960.2:p.Asn383=
ENST00000652672.1:c.1007A= ENSP00000498906.1:p.Asn336=
ENST00000352993.7:c.670+1463A= ENSP00000312236.5:n.670+1463A=
ENST00000354071.7:c.1148A= ENSP00000326002.7:p.Asn383=
ENST00000357654.7:c.1148A= ENSP00000350283.3:p.Asn383=
ENST00000412061.3:c.499A=
ENST00000461221.5:c.*931A= ENSP00000418548.1:n.*931A=
ENST00000468300.5:c.787+361A= ENSP00000417148.1:n.787+361A=
ENST00000470026.5:c.1148A= ENSP00000419274.1:p.Asn383=
ENST00000471181.6:c.1148A= ENSP00000418960.2:p.Asn383=
ENST00000473961.5:c.745A=
ENST00000477152.5:c.1070A= ENSP00000419988.1:p.Asn357=
ENST00000478531.5:c.784+361A= ENSP00000420412.1:n.784+361A=
ENST00000484087.5:c.409+361A= ENSP00000419481.1:n.409+361A=
ENST00000487825.5:c.412+361A= ENSP00000418212.1:n.412+361A=
ENST00000491747.6:c.787+361A= ENSP00000420705.2:n.787+361A=
ENST00000492859.5:c.*1084A= ENSP00000420253.1:n.*1084A=
ENST00000493795.5:c.1007A= ENSP00000418775.1:p.Asn336=
ENST00000493919.5:c.646+361A= ENSP00000418819.1:n.646+361A=
ENST00000494123.5:c.1148A= ENSP00000419103.1:p.Asn383=
ENST00000497488.1:c.260A= ENSP00000418986.1:p.Asn87=
ENST00000586385.5:c.5-30432A= ENSP00000465818.1:n.5-30432A=
ENST00000591534.5:c.-43-19862A= ENSP00000467329.1:n.-43-19862A=
ENST00000591849.5:c.-99+30888A= ENSP00000465347.1:n.-99+30888A=
ENST00000634433.1:c.1025A= ENSP00000489431.1:p.Asn342=
NM_007294.3:c.1148A= , LRG_292t1:c.1148A= NP_009225.1:p.Asn383=
NM_007297.3:c.1007A= NP_009228.2:p.Asn336=
NM_007298.3:c.787+361A= NP_009229.2:n.787+361A=
NM_007299.3:c.787+361A= NP_009230.2:n.787+361A=
NM_007300.3:c.1148A= NP_009231.2:p.Asn383=
NR_027676.1:n.1284A=
NM_007294.4:c.1148A= MANE Select NP_009225.1:p.Asn383=
NM_007297.4:c.1007A= NP_009228.2:p.Asn336=
NM_007299.4:c.787+361A= NP_009230.2:n.787+361A=
NM_007300.4:c.1148A= NP_009231.2:p.Asn383=
NR_027676.2:n.1325A=