Canonical Allele Identifier: CA002812
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 37586
dbSNP Id: rs397507229

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43076585del , CM000679.2:g.43076585del GRCh38
NC_000017.10:g.41228602del , CM000679.1:g.41228602del GRCh37
NC_000017.9:g.38482128del NCBI36
NG_005905.2:g.141399del , LRG_292:g.141399del

Transcript Alleles

HGVS Amino-acid change
ENST00000461574.2:c.4384del ENSP00000417241.2:p.Tyr1462ThrfsTer3
ENST00000470026.6:c.4387del ENSP00000419274.2:p.Tyr1463ThrfsTer3
ENST00000473961.6:c.4261del ENSP00000420201.2:p.Tyr1421ThrfsTer3
ENST00000476777.6:c.4381del ENSP00000417554.2:p.Tyr1461ThrfsTer3
ENST00000477152.6:c.4309del ENSP00000419988.2:p.Tyr1437ThrfsTer3
ENST00000478531.6:c.1075del ENSP00000420412.2:p.Tyr359ThrfsTer3
ENST00000489037.2:c.4309del ENSP00000420781.2:p.Tyr1437ThrfsTer3
ENST00000493919.6:c.937del ENSP00000418819.2:p.Tyr313ThrfsTer3
ENST00000494123.6:c.4387del ENSP00000419103.2:p.Tyr1463ThrfsTer3
ENST00000497488.2:c.3499del ENSP00000418986.2:p.Tyr1167ThrfsTer3
ENST00000618469.2:c.4387del ENSP00000478114.2:p.Tyr1463ThrfsTer3
ENST00000634433.2:c.4264del ENSP00000489431.2:p.Tyr1422ThrfsTer3
ENST00000644379.2:c.4453del ENSP00000496570.2:p.Tyr1485ThrfsTer3
ENST00000644555.2:c.937del ENSP00000494614.2:p.Tyr313ThrfsTer3
ENST00000652672.2:c.4246del ENSP00000498906.2:p.Tyr1416ThrfsTer3
ENST00000484087.6:c.949del ENSP00000419481.2:p.Tyr317ThrfsTer3
ENST00000700182.1:c.994del ENSP00000514849.1:p.Tyr332ThrfsTer3
ENST00000357654.9:c.4387del MANE Select ENSP00000350283.3:p.Tyr1463ThrfsTer3
ENST00000471181.7:c.4450del ENSP00000418960.2:p.Tyr1484ThrfsTer3
ENST00000644379.1:c.774del
ENST00000352993.7:c.961del ENSP00000312236.5:p.Tyr321ThrfsTer3
ENST00000357654.7:c.4387del ENSP00000350283.3:p.Tyr1463ThrfsTer3
ENST00000461221.5:c.*4170del ENSP00000418548.1:n.*4170del
ENST00000461574.1:c.678del
ENST00000468300.5:c.1075del ENSP00000417148.1:p.Tyr359ThrfsTer3
ENST00000471181.6:c.4450del ENSP00000418960.2:p.Tyr1484ThrfsTer3
ENST00000478531.5:c.1075del ENSP00000420412.1:p.Tyr359ThrfsTer3
ENST00000484087.5:c.700del ENSP00000419481.1:p.Tyr234ThrfsTer3
ENST00000487825.5:c.703del ENSP00000418212.1:p.Tyr235ThrfsTer3
ENST00000491747.6:c.1075del ENSP00000420705.2:p.Tyr359ThrfsTer3
ENST00000493795.5:c.4246del ENSP00000418775.1:p.Tyr1416ThrfsTer3
ENST00000493919.5:c.937del ENSP00000418819.1:p.Tyr313ThrfsTer3
ENST00000586385.5:c.5-12634del ENSP00000465818.1:n.5-12634del
ENST00000591534.5:c.-43-2064del ENSP00000467329.1:n.-43-2064del
ENST00000591849.5:c.-98-26395del ENSP00000465347.1:n.-98-26395del
ENST00000621897.1:n.278del
NM_007294.3:c.4387del , LRG_292t1:c.4387del NP_009225.1:p.Tyr1463ThrfsTer3
NM_007297.3:c.4246del NP_009228.2:p.Tyr1416ThrfsTer3
NM_007298.3:c.1075del NP_009229.2:p.Tyr359ThrfsTer3
NM_007299.3:c.1075del NP_009230.2:p.Tyr359ThrfsTer3
NM_007300.3:c.4450del NP_009231.2:p.Tyr1484ThrfsTer3
NR_027676.1:n.4523del
NM_007294.4:c.4387del MANE Select NP_009225.1:p.Tyr1463ThrfsTer3
NM_007297.4:c.4246del NP_009228.2:p.Tyr1416ThrfsTer3
NM_007299.4:c.1075del NP_009230.2:p.Tyr359ThrfsTer3
NM_007300.4:c.4450del NP_009231.2:p.Tyr1484ThrfsTer3
NR_027676.2:n.4564del