Canonical Allele Identifier: CA000946
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 54243
ClinVar RCV Id: RCV000256662
dbSNP Id: rs397508870

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094129del , CM000679.2:g.43094129del GRCh38
NC_000017.10:g.41246146del , CM000679.1:g.41246146del GRCh37
NC_000017.9:g.38499672del NCBI36
NG_005905.2:g.123856del , LRG_292:g.123856del

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.1467del
ENST00000461574.2:c.1403del ENSP00000417241.2:p.Lys468ArgfsTer7
ENST00000470026.6:c.1403del ENSP00000419274.2:p.Lys468ArgfsTer7
ENST00000473961.6:c.1277del ENSP00000420201.2:p.Lys426ArgfsTer7
ENST00000476777.6:c.1400del ENSP00000417554.2:p.Lys467ArgfsTer7
ENST00000477152.6:c.1325del ENSP00000419988.2:p.Lys442ArgfsTer7
ENST00000478531.6:c.784+616del ENSP00000420412.2:n.784+616del
ENST00000489037.2:c.1325del ENSP00000420781.2:p.Lys442ArgfsTer7
ENST00000493919.6:c.646+616del ENSP00000418819.2:n.646+616del
ENST00000494123.6:c.1403del ENSP00000419103.2:p.Lys468ArgfsTer7
ENST00000497488.2:c.515del ENSP00000418986.2:p.Lys172ArgfsTer7
ENST00000618469.2:c.1403del ENSP00000478114.2:p.Lys468ArgfsTer7
ENST00000634433.2:c.1280del ENSP00000489431.2:p.Lys427ArgfsTer7
ENST00000644379.2:c.1403del ENSP00000496570.2:p.Lys468ArgfsTer7
ENST00000644555.2:c.646+616del ENSP00000494614.2:n.646+616del
ENST00000652672.2:c.1262del ENSP00000498906.2:p.Lys421ArgfsTer7
ENST00000484087.6:c.664+616del ENSP00000419481.2:n.664+616del
ENST00000700182.1:c.706+616del ENSP00000514849.1:n.706+616del
ENST00000700183.1:c.*1411del ENSP00000514850.1:n.*1411del
ENST00000357654.9:c.1403del MANE Select ENSP00000350283.3:p.Lys468ArgfsTer7
ENST00000471181.7:c.1403del ENSP00000418960.2:p.Lys468ArgfsTer7
ENST00000652672.1:c.1262del ENSP00000498906.1:p.Lys421ArgfsTer7
ENST00000352993.7:c.670+1718del ENSP00000312236.5:n.670+1718del
ENST00000354071.7:c.1403del ENSP00000326002.7:p.Lys468ArgfsTer7
ENST00000357654.7:c.1403del ENSP00000350283.3:p.Lys468ArgfsTer7
ENST00000412061.3:c.754del
ENST00000461221.5:c.*1186del ENSP00000418548.1:n.*1186del
ENST00000468300.5:c.787+616del ENSP00000417148.1:n.787+616del
ENST00000470026.5:c.1403del ENSP00000419274.1:p.Lys468ArgfsTer7
ENST00000471181.6:c.1403del ENSP00000418960.2:p.Lys468ArgfsTer7
ENST00000477152.5:c.1325del ENSP00000419988.1:p.Lys442ArgfsTer7
ENST00000478531.5:c.784+616del ENSP00000420412.1:n.784+616del
ENST00000484087.5:c.409+616del ENSP00000419481.1:n.409+616del
ENST00000487825.5:c.412+616del ENSP00000418212.1:n.412+616del
ENST00000491747.6:c.787+616del ENSP00000420705.2:n.787+616del
ENST00000492859.5:c.*1339del ENSP00000420253.1:n.*1339del
ENST00000493795.5:c.1262del ENSP00000418775.1:p.Lys421ArgfsTer7
ENST00000493919.5:c.646+616del ENSP00000418819.1:n.646+616del
ENST00000494123.5:c.1403del ENSP00000419103.1:p.Lys468ArgfsTer?
ENST00000497488.1:c.515del ENSP00000418986.1:p.Lys172ArgfsTer?
ENST00000586385.5:c.5-30177del ENSP00000465818.1:n.5-30177del
ENST00000591534.5:c.-43-19607del ENSP00000467329.1:n.-43-19607del
ENST00000591849.5:c.-99+31143del ENSP00000465347.1:n.-99+31143del
ENST00000634433.1:c.1280del ENSP00000489431.1:p.Lys427ArgfsTer7
NM_007294.3:c.1403del , LRG_292t1:c.1403del NP_009225.1:p.Lys468ArgfsTer7
NM_007297.3:c.1262del NP_009228.2:p.Lys421ArgfsTer7
NM_007298.3:c.787+616del NP_009229.2:n.787+616del
NM_007299.3:c.787+616del NP_009230.2:n.787+616del
NM_007300.3:c.1403del NP_009231.2:p.Lys468ArgfsTer7
NR_027676.1:n.1539del
NM_007294.4:c.1403del MANE Select NP_009225.1:p.Lys468ArgfsTer7
NM_007297.4:c.1262del NP_009228.2:p.Lys421ArgfsTer7
NM_007299.4:c.787+616del NP_009230.2:n.787+616del
NM_007300.4:c.1403del NP_009231.2:p.Lys468ArgfsTer7
NR_027676.2:n.1580del