Canonical Allele Identifier: CA2260782115
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091641_43091642delinsGA , CM000679.2:g.43091641_43091642delinsGA GRCh38
NC_000017.10:g.41243658_41243659delinsGA , CM000679.1:g.41243658_41243659delinsGA GRCh37
NC_000017.9:g.38497184_38497185delinsGA NCBI36
NG_005905.2:g.126342_126343delinsTC , LRG_292:g.126342_126343delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3953_3954delinsTC
ENST00000461574.2:c.3889_3890delinsTC ENSP00000417241.2:p.Ser1297=
ENST00000470026.6:c.3889_3890delinsTC ENSP00000419274.2:p.Ser1297=
ENST00000473961.6:c.3763_3764delinsTC ENSP00000420201.2:p.Ser1255=
ENST00000476777.6:c.3886_3887delinsTC ENSP00000417554.2:p.Ser1296=
ENST00000477152.6:c.3811_3812delinsTC ENSP00000419988.2:p.Ser1271=
ENST00000478531.6:c.785-610_785-609delinsTC ENSP00000420412.2:n.785-610_785-609delinsTC
ENST00000489037.2:c.3811_3812delinsTC ENSP00000420781.2:p.Ser1271=
ENST00000493919.6:c.647-610_647-609delinsTC ENSP00000418819.2:n.647-610_647-609delinsTC
ENST00000494123.6:c.3889_3890delinsTC ENSP00000419103.2:p.Ser1297=
ENST00000497488.2:c.3001_3002delinsTC ENSP00000418986.2:p.Ser1001=
ENST00000618469.2:c.3889_3890delinsTC ENSP00000478114.2:p.Ser1297=
ENST00000634433.2:c.3766_3767delinsTC ENSP00000489431.2:p.Ser1256=
ENST00000644379.2:c.3889_3890delinsTC ENSP00000496570.2:p.Ser1297=
ENST00000644555.2:c.647-610_647-609delinsTC ENSP00000494614.2:n.647-610_647-609delinsTC
ENST00000652672.2:c.3748_3749delinsTC ENSP00000498906.2:p.Ser1250=
ENST00000484087.6:c.665-610_665-609delinsTC ENSP00000419481.2:n.665-610_665-609delinsTC
ENST00000700182.1:c.707-610_707-609delinsTC ENSP00000514849.1:n.707-610_707-609delinsTC
ENST00000357654.9:c.3889_3890delinsTC MANE Select ENSP00000350283.3:p.Ser1297=
ENST00000471181.7:c.3889_3890delinsTC ENSP00000418960.2:p.Ser1297=
ENST00000644379.1:c.210_211delinsTC
ENST00000352993.7:c.671-610_671-609delinsTC ENSP00000312236.5:n.671-610_671-609delinsTC
ENST00000354071.7:c.3889_3890delinsTC ENSP00000326002.7:p.Ser1297=
ENST00000357654.7:c.3889_3890delinsTC ENSP00000350283.3:p.Ser1297=
ENST00000461221.5:c.*3672_*3673delinsTC ENSP00000418548.1:n.*3672_*3673delinsTC
ENST00000461574.1:c.183_184delinsTC
ENST00000468300.5:c.788-610_788-609delinsTC ENSP00000417148.1:n.788-610_788-609delinsTC
ENST00000471181.6:c.3889_3890delinsTC ENSP00000418960.2:p.Ser1297=
ENST00000478531.5:c.785-610_785-609delinsTC ENSP00000420412.1:n.785-610_785-609delinsTC
ENST00000484087.5:c.410-610_410-609delinsTC ENSP00000419481.1:n.410-610_410-609delinsTC
ENST00000487825.5:c.413-610_413-609delinsTC ENSP00000418212.1:n.413-610_413-609delinsTC
ENST00000491747.6:c.788-610_788-609delinsTC ENSP00000420705.2:n.788-610_788-609delinsTC
ENST00000493795.5:c.3748_3749delinsTC ENSP00000418775.1:p.Ser1250=
ENST00000493919.5:c.647-610_647-609delinsTC ENSP00000418819.1:n.647-610_647-609delinsTC
ENST00000586385.5:c.5-27691_5-27690delinsTC ENSP00000465818.1:n.5-27691_5-27690delinsTC
ENST00000591534.5:c.-43-17121_-43-17120delinsTC ENSP00000467329.1:n.-43-17121_-43-17120delinsTC
ENST00000591849.5:c.-99+33629_-99+33630delinsTC ENSP00000465347.1:n.-99+33629_-99+33630delinsTC
NM_007294.3:c.3889_3890delinsTC , LRG_292t1:c.3889_3890delinsTC NP_009225.1:p.Ser1297=
NM_007297.3:c.3748_3749delinsTC NP_009228.2:p.Ser1250=
NM_007298.3:c.788-610_788-609delinsTC NP_009229.2:n.788-610_788-609delinsTC
NM_007299.3:c.788-610_788-609delinsTC NP_009230.2:n.788-610_788-609delinsTC
NM_007300.3:c.3889_3890delinsTC NP_009231.2:p.Ser1297=
NR_027676.1:n.4025_4026delinsTC
NM_007294.4:c.3889_3890delinsTC MANE Select NP_009225.1:p.Ser1297=
NM_007297.4:c.3748_3749delinsTC NP_009228.2:p.Ser1250=
NM_007299.4:c.788-610_788-609delinsTC NP_009230.2:n.788-610_788-609delinsTC
NM_007300.4:c.3889_3890delinsTC NP_009231.2:p.Ser1297=
NR_027676.2:n.4066_4067delinsTC