Canonical Allele Identifier: CA16615436
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 409302
dbSNP Id: rs1060502327

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43099878del , CM000679.2:g.43099878del GRCh38
NC_000017.10:g.41251895del , CM000679.1:g.41251895del GRCh37
NC_000017.9:g.38505421del NCBI36
NG_005905.2:g.118107del , LRG_292:g.118107del

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.509del
ENST00000461574.2:c.445del ENSP00000417241.2:p.Glu149LysfsTer14
ENST00000470026.6:c.445del ENSP00000419274.2:p.Glu149LysfsTer14
ENST00000473961.6:c.442del
ENST00000476777.6:c.442del
ENST00000477152.6:c.367del ENSP00000419988.2:p.Glu123LysfsTer14
ENST00000478531.6:c.442del
ENST00000489037.2:c.367del ENSP00000420781.2:p.Glu123LysfsTer14
ENST00000493919.6:c.304del ENSP00000418819.2:p.Glu102LysfsTer14
ENST00000494123.6:c.445del ENSP00000419103.2:p.Glu149LysfsTer14
ENST00000497488.2:c.-218-5017del ENSP00000418986.2:n.-218-5017del
ENST00000618469.2:c.445del ENSP00000478114.2:p.Glu149LysfsTer14
ENST00000634433.2:c.445del ENSP00000489431.2:p.Glu149LysfsTer14
ENST00000644379.2:c.445del ENSP00000496570.2:p.Glu149LysfsTer14
ENST00000644555.2:c.304del ENSP00000494614.2:p.Glu102LysfsTer14
ENST00000652672.2:c.304del ENSP00000498906.2:p.Glu102LysfsTer14
ENST00000484087.6:c.445del ENSP00000419481.2:p.Glu149LysfsTer14
ENST00000700182.1:c.364del
ENST00000700183.1:c.*359del ENSP00000514850.1:n.*359del
ENST00000700184.1:n.685del
ENST00000357654.9:c.445del MANE Select ENSP00000350283.3:p.Glu149LysfsTer14
ENST00000471181.7:c.445del ENSP00000418960.2:p.Glu149LysfsTer14
ENST00000642945.1:c.*319del ENSP00000495897.1:n.*319del
ENST00000652672.1:c.304del ENSP00000498906.1:p.Glu102LysfsTer14
ENST00000352993.7:c.445del ENSP00000312236.5:p.Glu149LysfsTer14
ENST00000354071.7:c.445del ENSP00000326002.7:p.Glu149LysfsTer14
ENST00000357654.7:c.445del ENSP00000350283.3:p.Glu149LysfsTer14
ENST00000461221.5:c.*228del
ENST00000461798.5:c.*231del ENSP00000417988.1:n.*231del
ENST00000468300.5:c.445del ENSP00000417148.1:p.Glu149LysfsTer14
ENST00000470026.5:c.445del ENSP00000419274.1:p.Glu149LysfsTer14
ENST00000471181.6:c.445del ENSP00000418960.2:p.Glu149LysfsTer14
ENST00000473961.5:c.165del
ENST00000476777.5:c.442del
ENST00000477152.5:c.367del ENSP00000419988.1:p.Glu123LysfsTer14
ENST00000478531.5:c.442del
ENST00000484087.5:c.190del
ENST00000487825.5:c.193del ENSP00000418212.1:p.Glu65LysfsTer14
ENST00000491747.6:c.445del ENSP00000420705.2:p.Glu149LysfsTer14
ENST00000492859.5:c.*381del ENSP00000420253.1:n.*381del
ENST00000493795.5:c.304del ENSP00000418775.1:p.Glu102LysfsTer14
ENST00000493919.5:c.304del ENSP00000418819.1:p.Glu102LysfsTer14
ENST00000494123.5:c.445del ENSP00000419103.1:p.Glu149LysfsTer14
ENST00000497488.1:c.-218-5017del ENSP00000418986.1:n.-218-5017del
ENST00000586385.5:c.4+25305del ENSP00000465818.1:n.4+25305del
ENST00000591534.5:c.-43-25356del ENSP00000467329.1:n.-43-25356del
ENST00000591849.5:c.-99+25394del ENSP00000465347.1:n.-99+25394del
ENST00000634433.1:c.445del ENSP00000489431.1:p.Glu149LysfsTer14
NM_007294.3:c.445del , LRG_292t1:c.445del NP_009225.1:p.Glu149LysfsTer14
NM_007297.3:c.304del NP_009228.2:p.Glu102LysfsTer14
NM_007298.3:c.445del NP_009229.2:p.Glu149LysfsTer14
NM_007299.3:c.445del NP_009230.2:p.Glu149LysfsTer14
NM_007300.3:c.445del NP_009231.2:p.Glu149LysfsTer14
NR_027676.1:n.581del
NM_007294.4:c.445del MANE Select NP_009225.1:p.Glu149LysfsTer14
NM_007297.4:c.304del NP_009228.2:p.Glu102LysfsTer14
NM_007299.4:c.445del NP_009230.2:p.Glu149LysfsTer14
NM_007300.4:c.445del NP_009231.2:p.Glu149LysfsTer14
NR_027676.2:n.622del