Canonical Allele Identifier: CA2260784651
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094144_43094145delinsTC , CM000679.2:g.43094144_43094145delinsTC GRCh38
NC_000017.10:g.41246161_41246162delinsTC , CM000679.1:g.41246161_41246162delinsTC GRCh37
NC_000017.9:g.38499687_38499688delinsTC NCBI36
NG_005905.2:g.123839_123840delinsGA , LRG_292:g.123839_123840delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.1450_1451delinsGA
ENST00000461574.2:c.1386_1387delinsGA ENSP00000417241.2:p.Gly462=
ENST00000470026.6:c.1386_1387delinsGA ENSP00000419274.2:p.Gly462=
ENST00000473961.6:c.1260_1261delinsGA ENSP00000420201.2:p.Gly420=
ENST00000476777.6:c.1383_1384delinsGA ENSP00000417554.2:p.Gly461=
ENST00000477152.6:c.1308_1309delinsGA ENSP00000419988.2:p.Gly436=
ENST00000478531.6:c.784+599_784+600delinsGA ENSP00000420412.2:n.784+599_784+600delinsGA
ENST00000489037.2:c.1308_1309delinsGA ENSP00000420781.2:p.Gly436=
ENST00000493919.6:c.646+599_646+600delinsGA ENSP00000418819.2:n.646+599_646+600delinsGA
ENST00000494123.6:c.1386_1387delinsGA ENSP00000419103.2:p.Gly462=
ENST00000497488.2:c.498_499delinsGA ENSP00000418986.2:p.Gly166=
ENST00000618469.2:c.1386_1387delinsGA ENSP00000478114.2:p.Gly462=
ENST00000634433.2:c.1263_1264delinsGA ENSP00000489431.2:p.Gly421=
ENST00000644379.2:c.1386_1387delinsGA ENSP00000496570.2:p.Gly462=
ENST00000644555.2:c.646+599_646+600delinsGA ENSP00000494614.2:n.646+599_646+600delinsGA
ENST00000652672.2:c.1245_1246delinsGA ENSP00000498906.2:p.Gly415=
ENST00000484087.6:c.664+599_664+600delinsGA ENSP00000419481.2:n.664+599_664+600delinsGA
ENST00000700182.1:c.706+599_706+600delinsGA ENSP00000514849.1:n.706+599_706+600delinsGA
ENST00000700183.1:c.*1394_*1395delinsGA ENSP00000514850.1:n.*1394_*1395delinsGA
ENST00000357654.9:c.1386_1387delinsGA MANE Select ENSP00000350283.3:p.Gly462=
ENST00000471181.7:c.1386_1387delinsGA ENSP00000418960.2:p.Gly462=
ENST00000652672.1:c.1245_1246delinsGA ENSP00000498906.1:p.Gly415=
ENST00000352993.7:c.670+1701_670+1702delinsGA ENSP00000312236.5:n.670+1701_670+1702delinsGA
ENST00000354071.7:c.1386_1387delinsGA ENSP00000326002.7:p.Gly462=
ENST00000357654.7:c.1386_1387delinsGA ENSP00000350283.3:p.Gly462=
ENST00000412061.3:c.737_738delinsGA
ENST00000461221.5:c.*1169_*1170delinsGA ENSP00000418548.1:n.*1169_*1170delinsGA
ENST00000468300.5:c.787+599_787+600delinsGA ENSP00000417148.1:n.787+599_787+600delinsGA
ENST00000470026.5:c.1386_1387delinsGA ENSP00000419274.1:p.Gly462=
ENST00000471181.6:c.1386_1387delinsGA ENSP00000418960.2:p.Gly462=
ENST00000477152.5:c.1308_1309delinsGA ENSP00000419988.1:p.Gly436=
ENST00000478531.5:c.784+599_784+600delinsGA ENSP00000420412.1:n.784+599_784+600delinsGA
ENST00000484087.5:c.409+599_409+600delinsGA ENSP00000419481.1:n.409+599_409+600delinsGA
ENST00000487825.5:c.412+599_412+600delinsGA ENSP00000418212.1:n.412+599_412+600delinsGA
ENST00000491747.6:c.787+599_787+600delinsGA ENSP00000420705.2:n.787+599_787+600delinsGA
ENST00000492859.5:c.*1322_*1323delinsGA ENSP00000420253.1:n.*1322_*1323delinsGA
ENST00000493795.5:c.1245_1246delinsGA ENSP00000418775.1:p.Gly415=
ENST00000493919.5:c.646+599_646+600delinsGA ENSP00000418819.1:n.646+599_646+600delinsGA
ENST00000494123.5:c.1386_1387delinsGA ENSP00000419103.1:p.Gly462=
ENST00000497488.1:c.498_499delinsGA ENSP00000418986.1:p.Gly166=
ENST00000586385.5:c.5-30194_5-30193delinsGA ENSP00000465818.1:n.5-30194_5-30193delinsGA
ENST00000591534.5:c.-43-19624_-43-19623delinsGA ENSP00000467329.1:n.-43-19624_-43-19623delinsGA
ENST00000591849.5:c.-99+31126_-99+31127delinsGA ENSP00000465347.1:n.-99+31126_-99+31127delinsGA
ENST00000634433.1:c.1263_1264delinsGA ENSP00000489431.1:p.Gly421=
NM_007294.3:c.1386_1387delinsGA , LRG_292t1:c.1386_1387delinsGA NP_009225.1:p.Gly462=
NM_007297.3:c.1245_1246delinsGA NP_009228.2:p.Gly415=
NM_007298.3:c.787+599_787+600delinsGA NP_009229.2:n.787+599_787+600delinsGA
NM_007299.3:c.787+599_787+600delinsGA NP_009230.2:n.787+599_787+600delinsGA
NM_007300.3:c.1386_1387delinsGA NP_009231.2:p.Gly462=
NR_027676.1:n.1522_1523delinsGA
NM_007294.4:c.1386_1387delinsGA MANE Select NP_009225.1:p.Gly462=
NM_007297.4:c.1245_1246delinsGA NP_009228.2:p.Gly415=
NM_007299.4:c.787+599_787+600delinsGA NP_009230.2:n.787+599_787+600delinsGA
NM_007300.4:c.1386_1387delinsGA NP_009231.2:p.Gly462=
NR_027676.2:n.1563_1564delinsGA