Canonical Allele Identifier: CA2260785343
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094857G= , CM000679.2:g.43094857G= GRCh38
NC_000017.10:g.41246874G= , CM000679.1:g.41246874G= GRCh37
NC_000017.9:g.38500400G= NCBI36
NG_005905.2:g.123127C= , LRG_292:g.123127C=

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.738C=
ENST00000461574.2:c.674C= ENSP00000417241.2:p.Ala225=
ENST00000470026.6:c.674C= ENSP00000419274.2:p.Ala225=
ENST00000473961.6:c.548C= ENSP00000420201.2:p.Ala183=
ENST00000476777.6:c.671C= ENSP00000417554.2:p.Ala224=
ENST00000477152.6:c.596C= ENSP00000419988.2:p.Ala199=
ENST00000478531.6:c.671C= ENSP00000420412.2:p.Ala224=
ENST00000489037.2:c.596C= ENSP00000420781.2:p.Ala199=
ENST00000493919.6:c.533C= ENSP00000418819.2:p.Ala178=
ENST00000494123.6:c.674C= ENSP00000419103.2:p.Ala225=
ENST00000497488.2:c.-215C= ENSP00000418986.2:n.-215C=
ENST00000618469.2:c.674C= ENSP00000478114.2:p.Ala225=
ENST00000634433.2:c.551C= ENSP00000489431.2:p.Ala184=
ENST00000644379.2:c.674C= ENSP00000496570.2:p.Ala225=
ENST00000644555.2:c.533C= ENSP00000494614.2:p.Ala178=
ENST00000652672.2:c.533C= ENSP00000498906.2:p.Ala178=
ENST00000484087.6:c.551C= ENSP00000419481.2:p.Ala184=
ENST00000700182.1:c.593C= ENSP00000514849.1:p.Ala198=
ENST00000700183.1:c.*682C= ENSP00000514850.1:n.*682C=
ENST00000357654.9:c.674C= MANE Select ENSP00000350283.3:p.Ala225=
ENST00000471181.7:c.674C= ENSP00000418960.2:p.Ala225=
ENST00000642945.1:c.*548C= ENSP00000495897.1:n.*548C=
ENST00000652672.1:c.533C= ENSP00000498906.1:p.Ala178=
ENST00000352993.7:c.670+989C= ENSP00000312236.5:n.670+989C=
ENST00000354071.7:c.674C= ENSP00000326002.7:p.Ala225=
ENST00000357654.7:c.674C= ENSP00000350283.3:p.Ala225=
ENST00000412061.3:c.25C=
ENST00000461221.5:c.*457C= ENSP00000418548.1:n.*457C=
ENST00000468300.5:c.674C= ENSP00000417148.1:p.Ala225=
ENST00000470026.5:c.674C= ENSP00000419274.1:p.Ala225=
ENST00000471181.6:c.674C= ENSP00000418960.2:p.Ala225=
ENST00000473961.5:c.271C=
ENST00000477152.5:c.596C= ENSP00000419988.1:p.Ala199=
ENST00000478531.5:c.671C= ENSP00000420412.1:p.Ala224=
ENST00000484087.5:c.296C= ENSP00000419481.1:p.Ala99=
ENST00000487825.5:c.299C= ENSP00000418212.1:p.Ala100=
ENST00000491747.6:c.674C= ENSP00000420705.2:p.Ala225=
ENST00000492859.5:c.*610C= ENSP00000420253.1:n.*610C=
ENST00000493795.5:c.533C= ENSP00000418775.1:p.Ala178=
ENST00000493919.5:c.533C= ENSP00000418819.1:p.Ala178=
ENST00000494123.5:c.674C= ENSP00000419103.1:p.Ala225=
ENST00000497488.1:c.-215C= ENSP00000418986.1:n.-215C=
ENST00000586385.5:c.4+30325C= ENSP00000465818.1:n.4+30325C=
ENST00000591534.5:c.-43-20336C= ENSP00000467329.1:n.-43-20336C=
ENST00000591849.5:c.-99+30414C= ENSP00000465347.1:n.-99+30414C=
ENST00000634433.1:c.551C= ENSP00000489431.1:p.Ala184=
NM_007294.3:c.674C= , LRG_292t1:c.674C= NP_009225.1:p.Ala225=
NM_007297.3:c.533C= NP_009228.2:p.Ala178=
NM_007298.3:c.674C= NP_009229.2:p.Ala225=
NM_007299.3:c.674C= NP_009230.2:p.Ala225=
NM_007300.3:c.674C= NP_009231.2:p.Ala225=
NR_027676.1:n.810C=
NM_007294.4:c.674C= MANE Select NP_009225.1:p.Ala225=
NM_007297.4:c.533C= NP_009228.2:p.Ala178=
NM_007299.4:c.674C= NP_009230.2:p.Ala225=
NM_007300.4:c.674C= NP_009231.2:p.Ala225=
NR_027676.2:n.851C=