Canonical Allele Identifier: CA000755
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 125488
ClinVar RCV Id: RCV003644906
dbSNP Id: rs80357776

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094402dup , CM000679.2:g.43094402dup GRCh38
NC_000017.10:g.41246419dup , CM000679.1:g.41246419dup GRCh37
NC_000017.9:g.38499945dup NCBI36
NG_005905.2:g.123582dup , LRG_292:g.123582dup

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.1193dup
ENST00000461574.2:c.1129dup ENSP00000417241.2:p.Ser377LysfsTer7
ENST00000470026.6:c.1129dup ENSP00000419274.2:p.Ser377LysfsTer7
ENST00000473961.6:c.1003dup ENSP00000420201.2:p.Ser335LysfsTer7
ENST00000476777.6:c.1126dup ENSP00000417554.2:p.Ser376LysfsTer7
ENST00000477152.6:c.1051dup ENSP00000419988.2:p.Ser351LysfsTer7
ENST00000478531.6:c.784+342dup ENSP00000420412.2:n.784+342dup
ENST00000489037.2:c.1051dup ENSP00000420781.2:p.Ser351LysfsTer7
ENST00000493919.6:c.646+342dup ENSP00000418819.2:n.646+342dup
ENST00000494123.6:c.1129dup ENSP00000419103.2:p.Ser377LysfsTer7
ENST00000497488.2:c.241dup ENSP00000418986.2:p.Ser81LysfsTer7
ENST00000618469.2:c.1129dup ENSP00000478114.2:p.Ser377LysfsTer7
ENST00000634433.2:c.1006dup ENSP00000489431.2:p.Ser336LysfsTer7
ENST00000644379.2:c.1129dup ENSP00000496570.2:p.Ser377LysfsTer7
ENST00000644555.2:c.646+342dup ENSP00000494614.2:n.646+342dup
ENST00000652672.2:c.988dup ENSP00000498906.2:p.Ser330LysfsTer7
ENST00000484087.6:c.664+342dup ENSP00000419481.2:n.664+342dup
ENST00000700182.1:c.706+342dup ENSP00000514849.1:n.706+342dup
ENST00000700183.1:c.*1137dup ENSP00000514850.1:n.*1137dup
ENST00000357654.9:c.1129dup MANE Select ENSP00000350283.3:p.Ser377LysfsTer7
ENST00000471181.7:c.1129dup ENSP00000418960.2:p.Ser377LysfsTer7
ENST00000652672.1:c.988dup ENSP00000498906.1:p.Ser330LysfsTer7
ENST00000352993.7:c.670+1444dup ENSP00000312236.5:n.670+1444dup
ENST00000354071.7:c.1129dup ENSP00000326002.7:p.Ser377LysfsTer7
ENST00000357654.7:c.1129dup ENSP00000350283.3:p.Ser377LysfsTer7
ENST00000412061.3:c.480dup
ENST00000461221.5:c.*912dup ENSP00000418548.1:n.*912dup
ENST00000468300.5:c.787+342dup ENSP00000417148.1:n.787+342dup
ENST00000470026.5:c.1129dup ENSP00000419274.1:p.Ser377LysfsTer7
ENST00000471181.6:c.1129dup ENSP00000418960.2:p.Ser377LysfsTer7
ENST00000473961.5:c.726dup
ENST00000477152.5:c.1051dup ENSP00000419988.1:p.Ser351LysfsTer7
ENST00000478531.5:c.784+342dup ENSP00000420412.1:n.784+342dup
ENST00000484087.5:c.409+342dup ENSP00000419481.1:n.409+342dup
ENST00000487825.5:c.412+342dup ENSP00000418212.1:n.412+342dup
ENST00000491747.6:c.787+342dup ENSP00000420705.2:n.787+342dup
ENST00000492859.5:c.*1065dup ENSP00000420253.1:n.*1065dup
ENST00000493795.5:c.988dup ENSP00000418775.1:p.Ser330LysfsTer7
ENST00000493919.5:c.646+342dup ENSP00000418819.1:n.646+342dup
ENST00000494123.5:c.1129dup ENSP00000419103.1:p.Ser377LysfsTer7
ENST00000497488.1:c.241dup ENSP00000418986.1:p.Ser81LysfsTer7
ENST00000586385.5:c.5-30451dup ENSP00000465818.1:n.5-30451dup
ENST00000591534.5:c.-43-19881dup ENSP00000467329.1:n.-43-19881dup
ENST00000591849.5:c.-99+30869dup ENSP00000465347.1:n.-99+30869dup
ENST00000634433.1:c.1006dup ENSP00000489431.1:p.Ser336LysfsTer7
NM_007294.3:c.1129dup , LRG_292t1:c.1129dup NP_009225.1:p.Ser377LysfsTer7
NM_007297.3:c.988dup NP_009228.2:p.Ser330LysfsTer7
NM_007298.3:c.787+342dup NP_009229.2:n.787+342dup
NM_007299.3:c.787+342dup NP_009230.2:n.787+342dup
NM_007300.3:c.1129dup NP_009231.2:p.Ser377LysfsTer7
NR_027676.1:n.1265dup
NM_007294.4:c.1129dup MANE Select NP_009225.1:p.Ser377LysfsTer7
NM_007297.4:c.988dup NP_009228.2:p.Ser330LysfsTer7
NM_007299.4:c.787+342dup NP_009230.2:n.787+342dup
NM_007300.4:c.1129dup NP_009231.2:p.Ser377LysfsTer7
NR_027676.2:n.1306dup