Canonical Allele Identifier: CA10598802
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1555591465

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093911C>A , CM000679.2:g.43093911C>A GRCh38
NC_000017.10:g.41245928C>A , CM000679.1:g.41245928C>A GRCh37
NC_000017.9:g.38499454C>A NCBI36
NG_005905.2:g.124073G>T , LRG_292:g.124073G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.1684G>T
ENST00000461574.2:c.1620G>T ENSP00000417241.2:p.Glu540Asp
ENST00000470026.6:c.1620G>T ENSP00000419274.2:p.Glu540Asp
ENST00000473961.6:c.1494G>T ENSP00000420201.2:p.Glu498Asp
ENST00000476777.6:c.1617G>T ENSP00000417554.2:p.Glu539Asp
ENST00000477152.6:c.1542G>T ENSP00000419988.2:p.Glu514Asp
ENST00000478531.6:c.784+833G>T ENSP00000420412.2:n.784+833G>T
ENST00000489037.2:c.1542G>T ENSP00000420781.2:p.Glu514Asp
ENST00000493919.6:c.646+833G>T ENSP00000418819.2:n.646+833G>T
ENST00000494123.6:c.1620G>T ENSP00000419103.2:p.Glu540Asp
ENST00000497488.2:c.732G>T ENSP00000418986.2:p.Glu244Asp
ENST00000618469.2:c.1620G>T ENSP00000478114.2:p.Glu540Asp
ENST00000634433.2:c.1497G>T ENSP00000489431.2:p.Glu499Asp
ENST00000644379.2:c.1620G>T ENSP00000496570.2:p.Glu540Asp
ENST00000644555.2:c.646+833G>T ENSP00000494614.2:n.646+833G>T
ENST00000652672.2:c.1479G>T ENSP00000498906.2:p.Glu493Asp
ENST00000484087.6:c.664+833G>T ENSP00000419481.2:n.664+833G>T
ENST00000700182.1:c.706+833G>T ENSP00000514849.1:n.706+833G>T
ENST00000357654.9:c.1620G>T MANE Select ENSP00000350283.3:p.Glu540Asp
ENST00000471181.7:c.1620G>T ENSP00000418960.2:p.Glu540Asp
ENST00000652672.1:c.1479G>T ENSP00000498906.1:p.Glu493Asp
ENST00000352993.7:c.670+1935G>T ENSP00000312236.5:n.670+1935G>T
ENST00000354071.7:c.1620G>T ENSP00000326002.7:p.Glu540Asp
ENST00000357654.7:c.1620G>T ENSP00000350283.3:p.Glu540Asp
ENST00000412061.3:c.971G>T
ENST00000461221.5:c.*1403G>T ENSP00000418548.1:n.*1403G>T
ENST00000468300.5:c.787+833G>T ENSP00000417148.1:n.787+833G>T
ENST00000470026.5:c.1620G>T ENSP00000419274.1:p.Glu540Asp
ENST00000471181.6:c.1620G>T ENSP00000418960.2:p.Glu540Asp
ENST00000477152.5:c.1542G>T ENSP00000419988.1:p.Glu514Asp
ENST00000478531.5:c.784+833G>T ENSP00000420412.1:n.784+833G>T
ENST00000484087.5:c.409+833G>T ENSP00000419481.1:n.409+833G>T
ENST00000487825.5:c.412+833G>T ENSP00000418212.1:n.412+833G>T
ENST00000491747.6:c.787+833G>T ENSP00000420705.2:n.787+833G>T
ENST00000493795.5:c.1479G>T ENSP00000418775.1:p.Glu493Asp
ENST00000493919.5:c.646+833G>T ENSP00000418819.1:n.646+833G>T
ENST00000586385.5:c.5-29960G>T ENSP00000465818.1:n.5-29960G>T
ENST00000591534.5:c.-43-19390G>T ENSP00000467329.1:n.-43-19390G>T
ENST00000591849.5:c.-99+31360G>T ENSP00000465347.1:n.-99+31360G>T
ENST00000634433.1:c.1497G>T ENSP00000489431.1:p.Glu499Asp
NM_007294.3:c.1620G>T , LRG_292t1:c.1620G>T NP_009225.1:p.Glu540Asp
NM_007297.3:c.1479G>T NP_009228.2:p.Glu493Asp
NM_007298.3:c.787+833G>T NP_009229.2:n.787+833G>T
NM_007299.3:c.787+833G>T NP_009230.2:n.787+833G>T
NM_007300.3:c.1620G>T NP_009231.2:p.Glu540Asp
NR_027676.1:n.1756G>T
NM_007294.4:c.1620G>T MANE Select NP_009225.1:p.Glu540Asp
NM_007297.4:c.1479G>T NP_009228.2:p.Glu493Asp
NM_007299.4:c.787+833G>T NP_009230.2:n.787+833G>T
NM_007300.4:c.1620G>T NP_009231.2:p.Glu540Asp
NR_027676.2:n.1797G>T