Canonical Allele Identifier: CA10589919
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 266188
ClinVar RCV Id: RCV000257450
dbSNP Id: rs886039968

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093735_43093738del , CM000679.2:g.43093735_43093738del GRCh38
NC_000017.10:g.41245752_41245755del , CM000679.1:g.41245752_41245755del GRCh37
NC_000017.9:g.38499278_38499281del NCBI36
NG_005905.2:g.124248_124251del , LRG_292:g.124248_124251del

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.1859_1862del
ENST00000461574.2:c.1795_1798del ENSP00000417241.2:p.Asn599SerfsTer12
ENST00000470026.6:c.1795_1798del ENSP00000419274.2:p.Asn599SerfsTer12
ENST00000473961.6:c.1669_1672del ENSP00000420201.2:p.Asn557SerfsTer12
ENST00000476777.6:c.1792_1795del ENSP00000417554.2:p.Asn598SerfsTer12
ENST00000477152.6:c.1717_1720del ENSP00000419988.2:p.Asn573SerfsTer12
ENST00000478531.6:c.784+1008_784+1011del ENSP00000420412.2:n.784+1008_784+1011del
ENST00000489037.2:c.1717_1720del ENSP00000420781.2:p.Asn573SerfsTer12
ENST00000493919.6:c.646+1008_646+1011del ENSP00000418819.2:n.646+1008_646+1011del
ENST00000494123.6:c.1795_1798del ENSP00000419103.2:p.Asn599SerfsTer12
ENST00000497488.2:c.907_910del ENSP00000418986.2:p.Asn303SerfsTer12
ENST00000618469.2:c.1795_1798del ENSP00000478114.2:p.Asn599SerfsTer12
ENST00000634433.2:c.1672_1675del ENSP00000489431.2:p.Asn558SerfsTer12
ENST00000644379.2:c.1795_1798del ENSP00000496570.2:p.Asn599SerfsTer12
ENST00000644555.2:c.646+1008_646+1011del ENSP00000494614.2:n.646+1008_646+1011del
ENST00000652672.2:c.1654_1657del ENSP00000498906.2:p.Asn552SerfsTer12
ENST00000484087.6:c.664+1008_664+1011del ENSP00000419481.2:n.664+1008_664+1011del
ENST00000700182.1:c.706+1008_706+1011del ENSP00000514849.1:n.706+1008_706+1011del
ENST00000357654.9:c.1795_1798del MANE Select ENSP00000350283.3:p.Asn599SerfsTer12
ENST00000471181.7:c.1795_1798del ENSP00000418960.2:p.Asn599SerfsTer12
ENST00000652672.1:c.1654_1657del ENSP00000498906.1:p.Asn552SerfsTer12
ENST00000352993.7:c.670+2110_670+2113del ENSP00000312236.5:n.670+2110_670+2113del
ENST00000354071.7:c.1795_1798del ENSP00000326002.7:p.Asn599SerfsTer12
ENST00000357654.7:c.1795_1798del ENSP00000350283.3:p.Asn599SerfsTer12
ENST00000412061.3:c.1146_1149del
ENST00000461221.5:c.*1578_*1581del ENSP00000418548.1:n.*1578_*1581del
ENST00000468300.5:c.787+1008_787+1011del ENSP00000417148.1:n.787+1008_787+1011del
ENST00000470026.5:c.1795_1798del ENSP00000419274.1:p.Asn599SerfsTer12
ENST00000471181.6:c.1795_1798del ENSP00000418960.2:p.Asn599SerfsTer12
ENST00000477152.5:c.1717_1720del ENSP00000419988.1:p.Asn573SerfsTer12
ENST00000478531.5:c.784+1008_784+1011del ENSP00000420412.1:n.784+1008_784+1011del
ENST00000484087.5:c.409+1008_409+1011del ENSP00000419481.1:n.409+1008_409+1011del
ENST00000487825.5:c.412+1008_412+1011del ENSP00000418212.1:n.412+1008_412+1011del
ENST00000491747.6:c.787+1008_787+1011del ENSP00000420705.2:n.787+1008_787+1011del
ENST00000493795.5:c.1654_1657del ENSP00000418775.1:p.Asn552SerfsTer12
ENST00000493919.5:c.646+1008_646+1011del ENSP00000418819.1:n.646+1008_646+1011del
ENST00000586385.5:c.5-29785_5-29782del ENSP00000465818.1:n.5-29785_5-29782del
ENST00000591534.5:c.-43-19215_-43-19212del ENSP00000467329.1:n.-43-19215_-43-19212de...
ENST00000591849.5:c.-99+31535_-99+31538del ENSP00000465347.1:n.-99+31535_-99+31538de...
ENST00000634433.1:c.1672_1675del ENSP00000489431.1:p.Asn558SerfsTer12
NM_007294.3:c.1795_1798del , LRG_292t1:c.1795_1798del NP_009225.1:p.Asn599SerfsTer12
NM_007297.3:c.1654_1657del NP_009228.2:p.Asn552SerfsTer12
NM_007298.3:c.787+1008_787+1011del NP_009229.2:n.787+1008_787+1011del
NM_007299.3:c.787+1008_787+1011del NP_009230.2:n.787+1008_787+1011del
NM_007300.3:c.1795_1798del NP_009231.2:p.Asn599SerfsTer12
NR_027676.1:n.1931_1934del
NM_007294.4:c.1795_1798del MANE Select NP_009225.1:p.Asn599SerfsTer12
NM_007297.4:c.1654_1657del NP_009228.2:p.Asn552SerfsTer12
NM_007299.4:c.787+1008_787+1011del NP_009230.2:n.787+1008_787+1011del
NM_007300.4:c.1795_1798del NP_009231.2:p.Asn599SerfsTer12
NR_027676.2:n.1972_1975del