Canonical Allele Identifier: CA2695225927
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076587del , CM000679.2:g.43076587del GRCh38
NC_000017.10:g.41228604del , CM000679.1:g.41228604del GRCh37
NC_000017.9:g.38482130del NCBI36
NG_005905.2:g.141398del , LRG_292:g.141398del

Transcript Alleles

HGVS Amino-acid Change
ENST00000461574.2:c.4383del ENSP00000417241.2:p.Glu1461AspfsTer4
ENST00000470026.6:c.4386del ENSP00000419274.2:p.Glu1462AspfsTer4
ENST00000473961.6:c.4260del ENSP00000420201.2:p.Glu1420AspfsTer4
ENST00000476777.6:c.4380del ENSP00000417554.2:p.Glu1460AspfsTer4
ENST00000477152.6:c.4308del ENSP00000419988.2:p.Glu1436AspfsTer4
ENST00000478531.6:c.1074del ENSP00000420412.2:p.Glu358AspfsTer4
ENST00000489037.2:c.4308del ENSP00000420781.2:p.Glu1436AspfsTer4
ENST00000493919.6:c.936del ENSP00000418819.2:p.Glu312AspfsTer4
ENST00000494123.6:c.4386del ENSP00000419103.2:p.Glu1462AspfsTer4
ENST00000497488.2:c.3498del ENSP00000418986.2:p.Glu1166AspfsTer4
ENST00000618469.2:c.4386del ENSP00000478114.2:p.Glu1462AspfsTer4
ENST00000634433.2:c.4263del ENSP00000489431.2:p.Glu1421AspfsTer4
ENST00000644379.2:c.4452del ENSP00000496570.2:p.Glu1484AspfsTer4
ENST00000644555.2:c.936del ENSP00000494614.2:p.Glu312AspfsTer4
ENST00000652672.2:c.4245del ENSP00000498906.2:p.Glu1415AspfsTer4
ENST00000484087.6:c.948del ENSP00000419481.2:p.Glu316AspfsTer4
ENST00000700182.1:c.993del ENSP00000514849.1:p.Glu331AspfsTer4
ENST00000357654.9:c.4386del MANE Select ENSP00000350283.3:p.Glu1462AspfsTer4
ENST00000471181.7:c.4449del ENSP00000418960.2:p.Glu1483AspfsTer4
ENST00000644379.1:c.773del
ENST00000352993.7:c.960del ENSP00000312236.5:p.Glu320AspfsTer4
ENST00000357654.7:c.4386del ENSP00000350283.3:p.Glu1462AspfsTer4
ENST00000461221.5:c.*4169del ENSP00000418548.1:n.*4169del
ENST00000461574.1:c.677del
ENST00000468300.5:c.1074del ENSP00000417148.1:p.Glu358AspfsTer4
ENST00000471181.6:c.4449del ENSP00000418960.2:p.Glu1483AspfsTer4
ENST00000478531.5:c.1074del ENSP00000420412.1:p.Glu358AspfsTer4
ENST00000484087.5:c.699del ENSP00000419481.1:p.Glu233AspfsTer4
ENST00000487825.5:c.702del ENSP00000418212.1:p.Glu234AspfsTer4
ENST00000491747.6:c.1074del ENSP00000420705.2:p.Glu358AspfsTer4
ENST00000493795.5:c.4245del ENSP00000418775.1:p.Glu1415AspfsTer4
ENST00000493919.5:c.936del ENSP00000418819.1:p.Glu312AspfsTer4
ENST00000586385.5:c.5-12635del ENSP00000465818.1:n.5-12635del
ENST00000591534.5:c.-43-2065del ENSP00000467329.1:n.-43-2065del
ENST00000591849.5:c.-98-26396del ENSP00000465347.1:n.-98-26396del
ENST00000621897.1:n.277del
NM_007294.3:c.4386del , LRG_292t1:c.4386del NP_009225.1:p.Glu1462AspfsTer4
NM_007297.3:c.4245del NP_009228.2:p.Glu1415AspfsTer4
NM_007298.3:c.1074del NP_009229.2:p.Glu358AspfsTer4
NM_007299.3:c.1074del NP_009230.2:p.Glu358AspfsTer4
NM_007300.3:c.4449del NP_009231.2:p.Glu1483AspfsTer4
NR_027676.1:n.4522del
NM_007294.4:c.4386del MANE Select NP_009225.1:p.Glu1462AspfsTer4
NM_007297.4:c.4245del NP_009228.2:p.Glu1415AspfsTer4
NM_007299.4:c.1074del NP_009230.2:p.Glu358AspfsTer4
NM_007300.4:c.4449del NP_009231.2:p.Glu1483AspfsTer4
NR_027676.2:n.4563del