Canonical Allele Identifier: CA2260784657
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094150_43094151delinsAT , CM000679.2:g.43094150_43094151delinsAT GRCh38
NC_000017.10:g.41246167_41246168delinsAT , CM000679.1:g.41246167_41246168delinsAT GRCh37
NC_000017.9:g.38499693_38499694delinsAT NCBI36
NG_005905.2:g.123833_123834delinsAT , LRG_292:g.123833_123834delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.1444_1445delinsAT
ENST00000461574.2:c.1380_1381delinsAT ENSP00000417241.2:p.Ile460=
ENST00000470026.6:c.1380_1381delinsAT ENSP00000419274.2:p.Ile460=
ENST00000473961.6:c.1254_1255delinsAT ENSP00000420201.2:p.Ile418=
ENST00000476777.6:c.1377_1378delinsAT ENSP00000417554.2:p.Ile459=
ENST00000477152.6:c.1302_1303delinsAT ENSP00000419988.2:p.Ile434=
ENST00000478531.6:c.784+593_784+594delinsAT ENSP00000420412.2:n.784+593_784+594delinsAT
ENST00000489037.2:c.1302_1303delinsAT ENSP00000420781.2:p.Ile434=
ENST00000493919.6:c.646+593_646+594delinsAT ENSP00000418819.2:n.646+593_646+594delinsAT
ENST00000494123.6:c.1380_1381delinsAT ENSP00000419103.2:p.Ile460=
ENST00000497488.2:c.492_493delinsAT ENSP00000418986.2:p.Ile164=
ENST00000618469.2:c.1380_1381delinsAT ENSP00000478114.2:p.Ile460=
ENST00000634433.2:c.1257_1258delinsAT ENSP00000489431.2:p.Ile419=
ENST00000644379.2:c.1380_1381delinsAT ENSP00000496570.2:p.Ile460=
ENST00000644555.2:c.646+593_646+594delinsAT ENSP00000494614.2:n.646+593_646+594delinsAT
ENST00000652672.2:c.1239_1240delinsAT ENSP00000498906.2:p.Ile413=
ENST00000484087.6:c.664+593_664+594delinsAT ENSP00000419481.2:n.664+593_664+594delinsAT
ENST00000700182.1:c.706+593_706+594delinsAT ENSP00000514849.1:n.706+593_706+594delinsAT
ENST00000700183.1:c.*1388_*1389delinsAT ENSP00000514850.1:n.*1388_*1389delinsAT
ENST00000357654.9:c.1380_1381delinsAT MANE Select ENSP00000350283.3:p.Ile460=
ENST00000471181.7:c.1380_1381delinsAT ENSP00000418960.2:p.Ile460=
ENST00000652672.1:c.1239_1240delinsAT ENSP00000498906.1:p.Ile413=
ENST00000352993.7:c.670+1695_670+1696delinsAT ENSP00000312236.5:n.670+1695_670+1696delinsAT
ENST00000354071.7:c.1380_1381delinsAT ENSP00000326002.7:p.Ile460=
ENST00000357654.7:c.1380_1381delinsAT ENSP00000350283.3:p.Ile460=
ENST00000412061.3:c.731_732delinsAT
ENST00000461221.5:c.*1163_*1164delinsAT ENSP00000418548.1:n.*1163_*1164delinsAT
ENST00000468300.5:c.787+593_787+594delinsAT ENSP00000417148.1:n.787+593_787+594delinsAT
ENST00000470026.5:c.1380_1381delinsAT ENSP00000419274.1:p.Ile460=
ENST00000471181.6:c.1380_1381delinsAT ENSP00000418960.2:p.Ile460=
ENST00000477152.5:c.1302_1303delinsAT ENSP00000419988.1:p.Ile434=
ENST00000478531.5:c.784+593_784+594delinsAT ENSP00000420412.1:n.784+593_784+594delinsAT
ENST00000484087.5:c.409+593_409+594delinsAT ENSP00000419481.1:n.409+593_409+594delinsAT
ENST00000487825.5:c.412+593_412+594delinsAT ENSP00000418212.1:n.412+593_412+594delinsAT
ENST00000491747.6:c.787+593_787+594delinsAT ENSP00000420705.2:n.787+593_787+594delinsAT
ENST00000492859.5:c.*1316_*1317delinsAT ENSP00000420253.1:n.*1316_*1317delinsAT
ENST00000493795.5:c.1239_1240delinsAT ENSP00000418775.1:p.Ile413=
ENST00000493919.5:c.646+593_646+594delinsAT ENSP00000418819.1:n.646+593_646+594delinsAT
ENST00000494123.5:c.1380_1381delinsAT ENSP00000419103.1:p.Ile460=
ENST00000497488.1:c.492_493delinsAT ENSP00000418986.1:p.Ile164=
ENST00000586385.5:c.5-30200_5-30199delinsAT ENSP00000465818.1:n.5-30200_5-30199delinsAT
ENST00000591534.5:c.-43-19630_-43-19629delinsAT ENSP00000467329.1:n.-43-19630_-43-19629delinsAT
ENST00000591849.5:c.-99+31120_-99+31121delinsAT ENSP00000465347.1:n.-99+31120_-99+31121delinsAT
ENST00000634433.1:c.1257_1258delinsAT ENSP00000489431.1:p.Ile419=
NM_007294.3:c.1380_1381delinsAT , LRG_292t1:c.1380_1381delinsAT NP_009225.1:p.Ile460=
NM_007297.3:c.1239_1240delinsAT NP_009228.2:p.Ile413=
NM_007298.3:c.787+593_787+594delinsAT NP_009229.2:n.787+593_787+594delinsAT
NM_007299.3:c.787+593_787+594delinsAT NP_009230.2:n.787+593_787+594delinsAT
NM_007300.3:c.1380_1381delinsAT NP_009231.2:p.Ile460=
NR_027676.1:n.1516_1517delinsAT
NM_007294.4:c.1380_1381delinsAT MANE Select NP_009225.1:p.Ile460=
NM_007297.4:c.1239_1240delinsAT NP_009228.2:p.Ile413=
NM_007299.4:c.787+593_787+594delinsAT NP_009230.2:n.787+593_787+594delinsAT
NM_007300.4:c.1380_1381delinsAT NP_009231.2:p.Ile460=
NR_027676.2:n.1557_1558delinsAT