Canonical Allele Identifier: CA2260784354
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093854_43093855delinsAC , CM000679.2:g.43093854_43093855delinsAC GRCh38
NC_000017.10:g.41245871_41245872delinsAC , CM000679.1:g.41245871_41245872delinsAC GRCh37
NC_000017.9:g.38499397_38499398delinsAC NCBI36
NG_005905.2:g.124129_124130delinsGT , LRG_292:g.124129_124130delinsGT

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.1740_1741delinsGT
ENST00000461574.2:c.1676_1677delinsGT ENSP00000417241.2:p.Gly559=
ENST00000470026.6:c.1676_1677delinsGT ENSP00000419274.2:p.Gly559=
ENST00000473961.6:c.1550_1551delinsGT ENSP00000420201.2:p.Gly517=
ENST00000476777.6:c.1673_1674delinsGT ENSP00000417554.2:p.Gly558=
ENST00000477152.6:c.1598_1599delinsGT ENSP00000419988.2:p.Gly533=
ENST00000478531.6:c.784+889_784+890delinsGT ENSP00000420412.2:n.784+889_784+890delins...
ENST00000489037.2:c.1598_1599delinsGT ENSP00000420781.2:p.Gly533=
ENST00000493919.6:c.646+889_646+890delinsGT ENSP00000418819.2:n.646+889_646+890delins...
ENST00000494123.6:c.1676_1677delinsGT ENSP00000419103.2:p.Gly559=
ENST00000497488.2:c.788_789delinsGT ENSP00000418986.2:p.Gly263=
ENST00000618469.2:c.1676_1677delinsGT ENSP00000478114.2:p.Gly559=
ENST00000634433.2:c.1553_1554delinsGT ENSP00000489431.2:p.Gly518=
ENST00000644379.2:c.1676_1677delinsGT ENSP00000496570.2:p.Gly559=
ENST00000644555.2:c.646+889_646+890delinsGT ENSP00000494614.2:n.646+889_646+890delins...
ENST00000652672.2:c.1535_1536delinsGT ENSP00000498906.2:p.Gly512=
ENST00000484087.6:c.664+889_664+890delinsGT ENSP00000419481.2:n.664+889_664+890delins...
ENST00000700182.1:c.706+889_706+890delinsGT ENSP00000514849.1:n.706+889_706+890delins...
ENST00000357654.9:c.1676_1677delinsGT MANE Select ENSP00000350283.3:p.Gly559=
ENST00000471181.7:c.1676_1677delinsGT ENSP00000418960.2:p.Gly559=
ENST00000652672.1:c.1535_1536delinsGT ENSP00000498906.1:p.Gly512=
ENST00000352993.7:c.670+1991_670+1992delinsGT ENSP00000312236.5:n.670+1991_670+1992deli...
ENST00000354071.7:c.1676_1677delinsGT ENSP00000326002.7:p.Gly559=
ENST00000357654.7:c.1676_1677delinsGT ENSP00000350283.3:p.Gly559=
ENST00000412061.3:c.1027_1028delinsGT
ENST00000461221.5:c.*1459_*1460delinsGT ENSP00000418548.1:n.*1459_*1460delinsGT
ENST00000468300.5:c.787+889_787+890delinsGT ENSP00000417148.1:n.787+889_787+890delins...
ENST00000470026.5:c.1676_1677delinsGT ENSP00000419274.1:p.Gly559=
ENST00000471181.6:c.1676_1677delinsGT ENSP00000418960.2:p.Gly559=
ENST00000477152.5:c.1598_1599delinsGT ENSP00000419988.1:p.Gly533=
ENST00000478531.5:c.784+889_784+890delinsGT ENSP00000420412.1:n.784+889_784+890delins...
ENST00000484087.5:c.409+889_409+890delinsGT ENSP00000419481.1:n.409+889_409+890delins...
ENST00000487825.5:c.412+889_412+890delinsGT ENSP00000418212.1:n.412+889_412+890delins...
ENST00000491747.6:c.787+889_787+890delinsGT ENSP00000420705.2:n.787+889_787+890delins...
ENST00000493795.5:c.1535_1536delinsGT ENSP00000418775.1:p.Gly512=
ENST00000493919.5:c.646+889_646+890delinsGT ENSP00000418819.1:n.646+889_646+890delins...
ENST00000586385.5:c.5-29904_5-29903delinsGT ENSP00000465818.1:n.5-29904_5-29903delins...
ENST00000591534.5:c.-43-19334_-43-19333delinsGT ENSP00000467329.1:n.-43-19334_-43-19333de...
ENST00000591849.5:c.-99+31416_-99+31417delinsGT ENSP00000465347.1:n.-99+31416_-99+31417de...
ENST00000634433.1:c.1553_1554delinsGT ENSP00000489431.1:p.Gly518=
NM_007294.3:c.1676_1677delinsGT , LRG_292t1:c.1676_1677delinsGT NP_009225.1:p.Gly559=
NM_007297.3:c.1535_1536delinsGT NP_009228.2:p.Gly512=
NM_007298.3:c.787+889_787+890delinsGT NP_009229.2:n.787+889_787+890delinsGT
NM_007299.3:c.787+889_787+890delinsGT NP_009230.2:n.787+889_787+890delinsGT
NM_007300.3:c.1676_1677delinsGT NP_009231.2:p.Gly559=
NR_027676.1:n.1812_1813delinsGT
NM_007294.4:c.1676_1677delinsGT MANE Select NP_009225.1:p.Gly559=
NM_007297.4:c.1535_1536delinsGT NP_009228.2:p.Gly512=
NM_007299.4:c.787+889_787+890delinsGT NP_009230.2:n.787+889_787+890delinsGT
NM_007300.4:c.1676_1677delinsGT NP_009231.2:p.Gly559=
NR_027676.2:n.1853_1854delinsGT