Canonical Allele Identifier: CA2260785168
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094665C= , CM000679.2:g.43094665C= GRCh38
NC_000017.10:g.41246682C= , CM000679.1:g.41246682C= GRCh37
NC_000017.9:g.38500208C= NCBI36
NG_005905.2:g.123319G= , LRG_292:g.123319G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.930G=
ENST00000461574.2:c.866G= ENSP00000417241.2:p.Ser289=
ENST00000470026.6:c.866G= ENSP00000419274.2:p.Ser289=
ENST00000473961.6:c.740G= ENSP00000420201.2:p.Ser247=
ENST00000476777.6:c.863G= ENSP00000417554.2:p.Ser288=
ENST00000477152.6:c.788G= ENSP00000419988.2:p.Ser263=
ENST00000478531.6:c.784+79G= ENSP00000420412.2:n.784+79G=
ENST00000489037.2:c.788G= ENSP00000420781.2:p.Ser263=
ENST00000493919.6:c.646+79G= ENSP00000418819.2:n.646+79G=
ENST00000494123.6:c.866G= ENSP00000419103.2:p.Ser289=
ENST00000497488.2:c.-23G= ENSP00000418986.2:n.-23G=
ENST00000618469.2:c.866G= ENSP00000478114.2:p.Ser289=
ENST00000634433.2:c.743G= ENSP00000489431.2:p.Ser248=
ENST00000644379.2:c.866G= ENSP00000496570.2:p.Ser289=
ENST00000644555.2:c.646+79G= ENSP00000494614.2:n.646+79G=
ENST00000652672.2:c.725G= ENSP00000498906.2:p.Ser242=
ENST00000484087.6:c.664+79G= ENSP00000419481.2:n.664+79G=
ENST00000700182.1:c.706+79G= ENSP00000514849.1:n.706+79G=
ENST00000700183.1:c.*874G= ENSP00000514850.1:n.*874G=
ENST00000357654.9:c.866G= MANE Select ENSP00000350283.3:p.Ser289=
ENST00000471181.7:c.866G= ENSP00000418960.2:p.Ser289=
ENST00000642945.1:c.*740G= ENSP00000495897.1:n.*740G=
ENST00000652672.1:c.725G= ENSP00000498906.1:p.Ser242=
ENST00000352993.7:c.670+1181G= ENSP00000312236.5:n.670+1181G=
ENST00000354071.7:c.866G= ENSP00000326002.7:p.Ser289=
ENST00000357654.7:c.866G= ENSP00000350283.3:p.Ser289=
ENST00000412061.3:c.217G=
ENST00000461221.5:c.*649G= ENSP00000418548.1:n.*649G=
ENST00000468300.5:c.787+79G= ENSP00000417148.1:n.787+79G=
ENST00000470026.5:c.866G= ENSP00000419274.1:p.Ser289=
ENST00000471181.6:c.866G= ENSP00000418960.2:p.Ser289=
ENST00000473961.5:c.463G=
ENST00000477152.5:c.788G= ENSP00000419988.1:p.Ser263=
ENST00000478531.5:c.784+79G= ENSP00000420412.1:n.784+79G=
ENST00000484087.5:c.409+79G= ENSP00000419481.1:n.409+79G=
ENST00000487825.5:c.412+79G= ENSP00000418212.1:n.412+79G=
ENST00000491747.6:c.787+79G= ENSP00000420705.2:n.787+79G=
ENST00000492859.5:c.*802G= ENSP00000420253.1:n.*802G=
ENST00000493795.5:c.725G= ENSP00000418775.1:p.Ser242=
ENST00000493919.5:c.646+79G= ENSP00000418819.1:n.646+79G=
ENST00000494123.5:c.866G= ENSP00000419103.1:p.Ser289=
ENST00000497488.1:c.-23G= ENSP00000418986.1:n.-23G=
ENST00000586385.5:c.4+30517G= ENSP00000465818.1:n.4+30517G=
ENST00000591534.5:c.-43-20144G= ENSP00000467329.1:n.-43-20144G=
ENST00000591849.5:c.-99+30606G= ENSP00000465347.1:n.-99+30606G=
ENST00000634433.1:c.743G= ENSP00000489431.1:p.Ser248=
NM_007294.3:c.866G= , LRG_292t1:c.866G= NP_009225.1:p.Ser289=
NM_007297.3:c.725G= NP_009228.2:p.Ser242=
NM_007298.3:c.787+79G= NP_009229.2:n.787+79G=
NM_007299.3:c.787+79G= NP_009230.2:n.787+79G=
NM_007300.3:c.866G= NP_009231.2:p.Ser289=
NR_027676.1:n.1002G=
NM_007294.4:c.866G= MANE Select NP_009225.1:p.Ser289=
NM_007297.4:c.725G= NP_009228.2:p.Ser242=
NM_007299.4:c.787+79G= NP_009230.2:n.787+79G=
NM_007300.4:c.866G= NP_009231.2:p.Ser289=
NR_027676.2:n.1043G=