Canonical Allele Identifier: CA2260784630
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43094125_43094126delinsGC , CM000679.2:g.43094125_43094126delinsGC GRCh38
NC_000017.10:g.41246142_41246143delinsGC , CM000679.1:g.41246142_41246143delinsGC GRCh37
NC_000017.9:g.38499668_38499669delinsGC NCBI36
NG_005905.2:g.123858_123859delinsGC , LRG_292:g.123858_123859delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.1469_1470delinsGC
ENST00000461574.2:c.1405_1406delinsGC ENSP00000417241.2:p.Ala469=
ENST00000470026.6:c.1405_1406delinsGC ENSP00000419274.2:p.Ala469=
ENST00000473961.6:c.1279_1280delinsGC ENSP00000420201.2:p.Ala427=
ENST00000476777.6:c.1402_1403delinsGC ENSP00000417554.2:p.Ala468=
ENST00000477152.6:c.1327_1328delinsGC ENSP00000419988.2:p.Ala443=
ENST00000478531.6:c.784+618_784+619delinsGC ENSP00000420412.2:n.784+618_784+619delinsGC
ENST00000489037.2:c.1327_1328delinsGC ENSP00000420781.2:p.Ala443=
ENST00000493919.6:c.646+618_646+619delinsGC ENSP00000418819.2:n.646+618_646+619delinsGC
ENST00000494123.6:c.1405_1406delinsGC ENSP00000419103.2:p.Ala469=
ENST00000497488.2:c.517_518delinsGC ENSP00000418986.2:p.Ala173=
ENST00000618469.2:c.1405_1406delinsGC ENSP00000478114.2:p.Ala469=
ENST00000634433.2:c.1282_1283delinsGC ENSP00000489431.2:p.Ala428=
ENST00000644379.2:c.1405_1406delinsGC ENSP00000496570.2:p.Ala469=
ENST00000644555.2:c.646+618_646+619delinsGC ENSP00000494614.2:n.646+618_646+619delinsGC
ENST00000652672.2:c.1264_1265delinsGC ENSP00000498906.2:p.Ala422=
ENST00000484087.6:c.664+618_664+619delinsGC ENSP00000419481.2:n.664+618_664+619delinsGC
ENST00000700182.1:c.706+618_706+619delinsGC ENSP00000514849.1:n.706+618_706+619delinsGC
ENST00000700183.1:c.*1413_*1414delinsGC ENSP00000514850.1:n.*1413_*1414delinsGC
ENST00000357654.9:c.1405_1406delinsGC MANE Select ENSP00000350283.3:p.Ala469=
ENST00000471181.7:c.1405_1406delinsGC ENSP00000418960.2:p.Ala469=
ENST00000652672.1:c.1264_1265delinsGC ENSP00000498906.1:p.Ala422=
ENST00000352993.7:c.670+1720_670+1721delinsGC ENSP00000312236.5:n.670+1720_670+1721delinsGC
ENST00000354071.7:c.1405_1406delinsGC ENSP00000326002.7:p.Ala469=
ENST00000357654.7:c.1405_1406delinsGC ENSP00000350283.3:p.Ala469=
ENST00000412061.3:c.756_757delinsGC
ENST00000461221.5:c.*1188_*1189delinsGC ENSP00000418548.1:n.*1188_*1189delinsGC
ENST00000468300.5:c.787+618_787+619delinsGC ENSP00000417148.1:n.787+618_787+619delinsGC
ENST00000470026.5:c.1405_1406delinsGC ENSP00000419274.1:p.Ala469=
ENST00000471181.6:c.1405_1406delinsGC ENSP00000418960.2:p.Ala469=
ENST00000477152.5:c.1327_1328delinsGC ENSP00000419988.1:p.Ala443=
ENST00000478531.5:c.784+618_784+619delinsGC ENSP00000420412.1:n.784+618_784+619delinsGC
ENST00000484087.5:c.409+618_409+619delinsGC ENSP00000419481.1:n.409+618_409+619delinsGC
ENST00000487825.5:c.412+618_412+619delinsGC ENSP00000418212.1:n.412+618_412+619delinsGC
ENST00000491747.6:c.787+618_787+619delinsGC ENSP00000420705.2:n.787+618_787+619delinsGC
ENST00000492859.5:c.*1341_*1342delinsGC ENSP00000420253.1:n.*1341_*1342delinsGC
ENST00000493795.5:c.1264_1265delinsGC ENSP00000418775.1:p.Ala422=
ENST00000493919.5:c.646+618_646+619delinsGC ENSP00000418819.1:n.646+618_646+619delinsGC
ENST00000494123.5:c.1405_1406delinsGC ENSP00000419103.1:p.Ala469=
ENST00000497488.1:c.517_518delinsGC ENSP00000418986.1:p.Ala173=
ENST00000586385.5:c.5-30175_5-30174delinsGC ENSP00000465818.1:n.5-30175_5-30174delinsGC
ENST00000591534.5:c.-43-19605_-43-19604delinsGC ENSP00000467329.1:n.-43-19605_-43-19604delinsGC
ENST00000591849.5:c.-99+31145_-99+31146delinsGC ENSP00000465347.1:n.-99+31145_-99+31146delinsGC
ENST00000634433.1:c.1282_1283delinsGC ENSP00000489431.1:p.Ala428=
NM_007294.3:c.1405_1406delinsGC , LRG_292t1:c.1405_1406delinsGC NP_009225.1:p.Ala469=
NM_007297.3:c.1264_1265delinsGC NP_009228.2:p.Ala422=
NM_007298.3:c.787+618_787+619delinsGC NP_009229.2:n.787+618_787+619delinsGC
NM_007299.3:c.787+618_787+619delinsGC NP_009230.2:n.787+618_787+619delinsGC
NM_007300.3:c.1405_1406delinsGC NP_009231.2:p.Ala469=
NR_027676.1:n.1541_1542delinsGC
NM_007294.4:c.1405_1406delinsGC MANE Select NP_009225.1:p.Ala469=
NM_007297.4:c.1264_1265delinsGC NP_009228.2:p.Ala422=
NM_007299.4:c.787+618_787+619delinsGC NP_009230.2:n.787+618_787+619delinsGC
NM_007300.4:c.1405_1406delinsGC NP_009231.2:p.Ala469=
NR_027676.2:n.1582_1583delinsGC