Canonical Allele Identifier: CA2260784297
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093759_43093762delinsATAC , CM000679.2:g.43093759_43093762delinsATAC GRCh38
NC_000017.10:g.41245776_41245779delinsATAC , CM000679.1:g.41245776_41245779delinsATAC GRCh37
NC_000017.9:g.38499302_38499305delinsATAC NCBI36
NG_005905.2:g.124222_124225delinsGTAT , LRG_292:g.124222_124225delinsGTAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.1833_1836delinsGTAT
ENST00000461574.2:c.1769_1772delinsGTAT ENSP00000417241.2:p.Ser590=
ENST00000470026.6:c.1769_1772delinsGTAT ENSP00000419274.2:p.Ser590=
ENST00000473961.6:c.1643_1646delinsGTAT ENSP00000420201.2:p.Ser548=
ENST00000476777.6:c.1766_1769delinsGTAT ENSP00000417554.2:p.Ser589=
ENST00000477152.6:c.1691_1694delinsGTAT ENSP00000419988.2:p.Ser564=
ENST00000478531.6:c.784+982_784+985delinsGTAT ENSP00000420412.2:n.784+982_784+985delinsGTAT
ENST00000489037.2:c.1691_1694delinsGTAT ENSP00000420781.2:p.Ser564=
ENST00000493919.6:c.646+982_646+985delinsGTAT ENSP00000418819.2:n.646+982_646+985delinsGTAT
ENST00000494123.6:c.1769_1772delinsGTAT ENSP00000419103.2:p.Ser590=
ENST00000497488.2:c.881_884delinsGTAT ENSP00000418986.2:p.Ser294=
ENST00000618469.2:c.1769_1772delinsGTAT ENSP00000478114.2:p.Ser590=
ENST00000634433.2:c.1646_1649delinsGTAT ENSP00000489431.2:p.Ser549=
ENST00000644379.2:c.1769_1772delinsGTAT ENSP00000496570.2:p.Ser590=
ENST00000644555.2:c.646+982_646+985delinsGTAT ENSP00000494614.2:n.646+982_646+985delinsGTAT
ENST00000652672.2:c.1628_1631delinsGTAT ENSP00000498906.2:p.Ser543=
ENST00000484087.6:c.664+982_664+985delinsGTAT ENSP00000419481.2:n.664+982_664+985delinsGTAT
ENST00000700182.1:c.706+982_706+985delinsGTAT ENSP00000514849.1:n.706+982_706+985delinsGTAT
ENST00000357654.9:c.1769_1772delinsGTAT MANE Select ENSP00000350283.3:p.Ser590=
ENST00000471181.7:c.1769_1772delinsGTAT ENSP00000418960.2:p.Ser590=
ENST00000652672.1:c.1628_1631delinsGTAT ENSP00000498906.1:p.Ser543=
ENST00000352993.7:c.670+2084_670+2087delinsGTAT ENSP00000312236.5:n.670+2084_670+2087delinsGTAT
ENST00000354071.7:c.1769_1772delinsGTAT ENSP00000326002.7:p.Ser590=
ENST00000357654.7:c.1769_1772delinsGTAT ENSP00000350283.3:p.Ser590=
ENST00000412061.3:c.1120_1123delinsGTAT
ENST00000461221.5:c.*1552_*1555delinsGTAT ENSP00000418548.1:n.*1552_*1555delinsGTAT
ENST00000468300.5:c.787+982_787+985delinsGTAT ENSP00000417148.1:n.787+982_787+985delinsGTAT
ENST00000470026.5:c.1769_1772delinsGTAT ENSP00000419274.1:p.Ser590=
ENST00000471181.6:c.1769_1772delinsGTAT ENSP00000418960.2:p.Ser590=
ENST00000477152.5:c.1691_1694delinsGTAT ENSP00000419988.1:p.Ser564=
ENST00000478531.5:c.784+982_784+985delinsGTAT ENSP00000420412.1:n.784+982_784+985delinsGTAT
ENST00000484087.5:c.409+982_409+985delinsGTAT ENSP00000419481.1:n.409+982_409+985delinsGTAT
ENST00000487825.5:c.412+982_412+985delinsGTAT ENSP00000418212.1:n.412+982_412+985delinsGTAT
ENST00000491747.6:c.787+982_787+985delinsGTAT ENSP00000420705.2:n.787+982_787+985delinsGTAT
ENST00000493795.5:c.1628_1631delinsGTAT ENSP00000418775.1:p.Ser543=
ENST00000493919.5:c.646+982_646+985delinsGTAT ENSP00000418819.1:n.646+982_646+985delinsGTAT
ENST00000586385.5:c.5-29811_5-29808delinsGTAT ENSP00000465818.1:n.5-29811_5-29808delinsGTAT
ENST00000591534.5:c.-43-19241_-43-19238delinsGTAT ENSP00000467329.1:n.-43-19241_-43-19238delinsGTAT
ENST00000591849.5:c.-99+31509_-99+31512delinsGTAT ENSP00000465347.1:n.-99+31509_-99+31512delinsGTAT
ENST00000634433.1:c.1646_1649delinsGTAT ENSP00000489431.1:p.Ser549=
NM_007294.3:c.1769_1772delinsGTAT , LRG_292t1:c.1769_1772delinsGTAT NP_009225.1:p.Ser590=
NM_007297.3:c.1628_1631delinsGTAT NP_009228.2:p.Ser543=
NM_007298.3:c.787+982_787+985delinsGTAT NP_009229.2:n.787+982_787+985delinsGTAT
NM_007299.3:c.787+982_787+985delinsGTAT NP_009230.2:n.787+982_787+985delinsGTAT
NM_007300.3:c.1769_1772delinsGTAT NP_009231.2:p.Ser590=
NR_027676.1:n.1905_1908delinsGTAT
NM_007294.4:c.1769_1772delinsGTAT MANE Select NP_009225.1:p.Ser590=
NM_007297.4:c.1628_1631delinsGTAT NP_009228.2:p.Ser543=
NM_007299.4:c.787+982_787+985delinsGTAT NP_009230.2:n.787+982_787+985delinsGTAT
NM_007300.4:c.1769_1772delinsGTAT NP_009231.2:p.Ser590=
NR_027676.2:n.1946_1949delinsGTAT