Canonical Allele Identifier: CA2809539034
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094086_43094087insGCAGTCTGCCCAC , CM000679.2:g.43094086_43094087insGCAGTCTGCCCAC GRCh38
NC_000017.10:g.41246103_41246104insGCAGTCTGCCCAC , CM000679.1:g.41246103_41246104insGCAGTCTGCCCAC GRCh37
NC_000017.9:g.38499629_38499630insGCAGTCTGCCCAC NCBI36
NG_005905.2:g.123897_123898insGTGGGCAGACTGC , LRG_292:g.123897_123898insGTGGGCAGACTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.1508_1509insGTGGGCAGACTGC
ENST00000461574.2:c.1444_1445insGTGGGCAGACTGC ENSP00000417241.2:p.Ile482SerfsTer12
ENST00000470026.6:c.1444_1445insGTGGGCAGACTGC ENSP00000419274.2:p.Ile482SerfsTer12
ENST00000473961.6:c.1318_1319insGTGGGCAGACTGC ENSP00000420201.2:p.Ile440SerfsTer12
ENST00000476777.6:c.1441_1442insGTGGGCAGACTGC ENSP00000417554.2:p.Ile481SerfsTer12
ENST00000477152.6:c.1366_1367insGTGGGCAGACTGC ENSP00000419988.2:p.Ile456SerfsTer12
ENST00000478531.6:c.784+657_784+658insGTGGGCAGACTGC ENSP00000420412.2:n.784+657_784+658insGTGGGCAGACTGC
ENST00000489037.2:c.1366_1367insGTGGGCAGACTGC ENSP00000420781.2:p.Ile456SerfsTer12
ENST00000493919.6:c.646+657_646+658insGTGGGCAGACTGC ENSP00000418819.2:n.646+657_646+658insGTGGGCAGACTGC
ENST00000494123.6:c.1444_1445insGTGGGCAGACTGC ENSP00000419103.2:p.Ile482SerfsTer12
ENST00000497488.2:c.556_557insGTGGGCAGACTGC ENSP00000418986.2:p.Ile186SerfsTer12
ENST00000618469.2:c.1444_1445insGTGGGCAGACTGC ENSP00000478114.2:p.Ile482SerfsTer12
ENST00000634433.2:c.1321_1322insGTGGGCAGACTGC ENSP00000489431.2:p.Ile441SerfsTer12
ENST00000644379.2:c.1444_1445insGTGGGCAGACTGC ENSP00000496570.2:p.Ile482SerfsTer12
ENST00000644555.2:c.646+657_646+658insGTGGGCAGACTGC ENSP00000494614.2:n.646+657_646+658insGTGGGCAGACTGC
ENST00000652672.2:c.1303_1304insGTGGGCAGACTGC ENSP00000498906.2:p.Ile435SerfsTer12
ENST00000484087.6:c.664+657_664+658insGTGGGCAGACTGC ENSP00000419481.2:n.664+657_664+658insGTGGGCAGACTGC
ENST00000700182.1:c.706+657_706+658insGTGGGCAGACTGC ENSP00000514849.1:n.706+657_706+658insGTGGGCAGACTGC
ENST00000700183.1:c.*1452_*1453insGTGGGCAGACTGC ENSP00000514850.1:n.*1452_*1453insGTGGGCAGACTGC
ENST00000357654.9:c.1444_1445insGTGGGCAGACTGC MANE Select ENSP00000350283.3:p.Ile482SerfsTer12
ENST00000471181.7:c.1444_1445insGTGGGCAGACTGC ENSP00000418960.2:p.Ile482SerfsTer12
ENST00000652672.1:c.1303_1304insGTGGGCAGACTGC ENSP00000498906.1:p.Ile435SerfsTer12
ENST00000352993.7:c.670+1759_670+1760insGTGGGCAGACTGC ENSP00000312236.5:n.670+1759_670+1760insGTGGGCAGACTGC
ENST00000354071.7:c.1444_1445insGTGGGCAGACTGC ENSP00000326002.7:p.Ile482SerfsTer12
ENST00000357654.7:c.1444_1445insGTGGGCAGACTGC ENSP00000350283.3:p.Ile482SerfsTer12
ENST00000412061.3:c.795_796insGTGGGCAGACTGC
ENST00000461221.5:c.*1227_*1228insGTGGGCAGACTGC ENSP00000418548.1:n.*1227_*1228insGTGGGCAGACTGC
ENST00000468300.5:c.787+657_787+658insGTGGGCAGACTGC ENSP00000417148.1:n.787+657_787+658insGTGGGCAGACTGC
ENST00000470026.5:c.1444_1445insGTGGGCAGACTGC ENSP00000419274.1:p.Ile482SerfsTer12
ENST00000471181.6:c.1444_1445insGTGGGCAGACTGC ENSP00000418960.2:p.Ile482SerfsTer12
ENST00000477152.5:c.1366_1367insGTGGGCAGACTGC ENSP00000419988.1:p.Ile456SerfsTer12
ENST00000478531.5:c.784+657_784+658insGTGGGCAGACTGC ENSP00000420412.1:n.784+657_784+658insGTGGGCAGACTGC
ENST00000484087.5:c.409+657_409+658insGTGGGCAGACTGC ENSP00000419481.1:n.409+657_409+658insGTGGGCAGACTGC
ENST00000487825.5:c.412+657_412+658insGTGGGCAGACTGC ENSP00000418212.1:n.412+657_412+658insGTGGGCAGACTGC
ENST00000491747.6:c.787+657_787+658insGTGGGCAGACTGC ENSP00000420705.2:n.787+657_787+658insGTGGGCAGACTGC
ENST00000493795.5:c.1303_1304insGTGGGCAGACTGC ENSP00000418775.1:p.Ile435SerfsTer12
ENST00000493919.5:c.646+657_646+658insGTGGGCAGACTGC ENSP00000418819.1:n.646+657_646+658insGTGGGCAGACTGC
ENST00000586385.5:c.5-30136_5-30135insGTGGGCAGACTGC ENSP00000465818.1:n.5-30136_5-30135insGTGGGCAGACTGC
ENST00000591534.5:c.-43-19566_-43-19565insGTGGGCAGACTGC ENSP00000467329.1:n.-43-19566_-43-19565insGTGGGCAGACTGC
ENST00000591849.5:c.-99+31184_-99+31185insGTGGGCAGACTGC ENSP00000465347.1:n.-99+31184_-99+31185insGTGGGCAGACTGC
ENST00000634433.1:c.1321_1322insGTGGGCAGACTGC ENSP00000489431.1:p.Ile441SerfsTer12
NM_007294.3:c.1444_1445insGTGGGCAGACTGC , LRG_292t1:c.1444_1445insGTGGGCAGACTGC NP_009225.1:p.Ile482SerfsTer12
NM_007297.3:c.1303_1304insGTGGGCAGACTGC NP_009228.2:p.Ile435SerfsTer12
NM_007298.3:c.787+657_787+658insGTGGGCAGACTGC NP_009229.2:n.787+657_787+658insGTGGGCAGACTGC
NM_007299.3:c.787+657_787+658insGTGGGCAGACTGC NP_009230.2:n.787+657_787+658insGTGGGCAGACTGC
NM_007300.3:c.1444_1445insGTGGGCAGACTGC NP_009231.2:p.Ile482SerfsTer12
NR_027676.1:n.1580_1581insGTGGGCAGACTGC
NM_007294.4:c.1444_1445insGTGGGCAGACTGC MANE Select NP_009225.1:p.Ile482SerfsTer12
NM_007297.4:c.1303_1304insGTGGGCAGACTGC NP_009228.2:p.Ile435SerfsTer12
NM_007299.4:c.787+657_787+658insGTGGGCAGACTGC NP_009230.2:n.787+657_787+658insGTGGGCAGACTGC
NM_007300.4:c.1444_1445insGTGGGCAGACTGC NP_009231.2:p.Ile482SerfsTer12
NR_027676.2:n.1621_1622insGTGGGCAGACTGC