Canonical Allele Identifier: CA2260766369
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43057058G= , CM000679.2:g.43057058G= GRCh38
NC_000017.10:g.41209075G= , CM000679.1:g.41209075G= GRCh37
NC_000017.9:g.38462601G= NCBI36
NG_005905.2:g.160926C= , LRG_292:g.160926C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.5268C= ENSP00000417241.2:p.Asp1756=
ENST00000470026.6:c.5271C= ENSP00000419274.2:p.Asp1757=
ENST00000473961.6:c.5145C= ENSP00000420201.2:p.Asp1715=
ENST00000476777.6:c.5265C= ENSP00000417554.2:p.Asp1755=
ENST00000477152.6:c.5193C= ENSP00000419988.2:p.Asp1731=
ENST00000478531.6:c.1959C= ENSP00000420412.2:p.Asp653=
ENST00000489037.2:c.5193C= ENSP00000420781.2:p.Asp1731=
ENST00000493919.6:c.1821C= ENSP00000418819.2:p.Asp607=
ENST00000494123.6:c.5271C= ENSP00000419103.2:p.Asp1757=
ENST00000497488.2:c.4383C= ENSP00000418986.2:p.Asp1461=
ENST00000618469.2:c.5271C= ENSP00000478114.2:p.Asp1757=
ENST00000634433.2:c.5148C= ENSP00000489431.2:p.Asp1716=
ENST00000644379.2:c.5337C= ENSP00000496570.2:p.Asp1779=
ENST00000644555.2:c.1821C= ENSP00000494614.2:p.Asp607=
ENST00000652672.2:c.5130C= ENSP00000498906.2:p.Asp1710=
ENST00000484087.6:c.1833C= ENSP00000419481.2:p.Asp611=
ENST00000357654.9:c.5271C= MANE Select ENSP00000350283.3:p.Asp1757=
ENST00000471181.7:c.5334C= ENSP00000418960.2:p.Asp1778=
ENST00000644379.1:c.1658C=
ENST00000352993.7:c.1845C= ENSP00000312236.5:p.Asp615=
ENST00000357654.7:c.5271C= ENSP00000350283.3:p.Asp1757=
ENST00000461221.5:c.*5054C= ENSP00000418548.1:n.*5054C=
ENST00000468300.5:c.1959C= ENSP00000417148.1:p.Asp653=
ENST00000471181.6:c.5334C= ENSP00000418960.2:p.Asp1778=
ENST00000491747.6:c.1959C= ENSP00000420705.2:p.Asp653=
ENST00000493795.5:c.5130C= ENSP00000418775.1:p.Asp1710=
ENST00000586385.5:c.201C= ENSP00000465818.1:p.Asp67=
ENST00000591534.5:c.744C= ENSP00000467329.1:p.Asp248=
ENST00000591849.5:c.-98-6868C= ENSP00000465347.1:n.-98-6868C=
NM_007294.3:c.5271C= , LRG_292t1:c.5271C= NP_009225.1:p.Asp1757=
NM_007297.3:c.5130C= NP_009228.2:p.Asp1710=
NM_007298.3:c.1959C= NP_009229.2:p.Asp653=
NM_007299.3:c.1959C= NP_009230.2:p.Asp653=
NM_007300.3:c.5334C= NP_009231.2:p.Asp1778=
NR_027676.1:n.5407C=
NM_007294.4:c.5271C= MANE Select NP_009225.1:p.Asp1757=
NM_007297.4:c.5130C= NP_009228.2:p.Asp1710=
NM_007299.4:c.1959C= NP_009230.2:p.Asp653=
NM_007300.4:c.5334C= NP_009231.2:p.Asp1778=
NR_027676.2:n.5448C=