Canonical Allele Identifier: CA2260782166
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091686_43091687delinsTC , CM000679.2:g.43091686_43091687delinsTC GRCh38
NC_000017.10:g.41243703_41243704delinsTC , CM000679.1:g.41243703_41243704delinsTC GRCh37
NC_000017.9:g.38497229_38497230delinsTC NCBI36
NG_005905.2:g.126297_126298delinsGA , LRG_292:g.126297_126298delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3908_3909delinsGA
ENST00000461574.2:c.3844_3845delinsGA ENSP00000417241.2:p.Glu1282=
ENST00000470026.6:c.3844_3845delinsGA ENSP00000419274.2:p.Glu1282=
ENST00000473961.6:c.3718_3719delinsGA ENSP00000420201.2:p.Glu1240=
ENST00000476777.6:c.3841_3842delinsGA ENSP00000417554.2:p.Glu1281=
ENST00000477152.6:c.3766_3767delinsGA ENSP00000419988.2:p.Glu1256=
ENST00000478531.6:c.785-655_785-654delinsGA ENSP00000420412.2:n.785-655_785-654delinsGA
ENST00000489037.2:c.3766_3767delinsGA ENSP00000420781.2:p.Glu1256=
ENST00000493919.6:c.647-655_647-654delinsGA ENSP00000418819.2:n.647-655_647-654delinsGA
ENST00000494123.6:c.3844_3845delinsGA ENSP00000419103.2:p.Glu1282=
ENST00000497488.2:c.2956_2957delinsGA ENSP00000418986.2:p.Glu986=
ENST00000618469.2:c.3844_3845delinsGA ENSP00000478114.2:p.Glu1282=
ENST00000634433.2:c.3721_3722delinsGA ENSP00000489431.2:p.Glu1241=
ENST00000644379.2:c.3844_3845delinsGA ENSP00000496570.2:p.Glu1282=
ENST00000644555.2:c.647-655_647-654delinsGA ENSP00000494614.2:n.647-655_647-654delinsGA
ENST00000652672.2:c.3703_3704delinsGA ENSP00000498906.2:p.Glu1235=
ENST00000484087.6:c.665-655_665-654delinsGA ENSP00000419481.2:n.665-655_665-654delinsGA
ENST00000700182.1:c.707-655_707-654delinsGA ENSP00000514849.1:n.707-655_707-654delinsGA
ENST00000357654.9:c.3844_3845delinsGA MANE Select ENSP00000350283.3:p.Glu1282=
ENST00000471181.7:c.3844_3845delinsGA ENSP00000418960.2:p.Glu1282=
ENST00000644379.1:c.165_166delinsGA
ENST00000352993.7:c.671-655_671-654delinsGA ENSP00000312236.5:n.671-655_671-654delinsGA
ENST00000354071.7:c.3844_3845delinsGA ENSP00000326002.7:p.Glu1282=
ENST00000357654.7:c.3844_3845delinsGA ENSP00000350283.3:p.Glu1282=
ENST00000461221.5:c.*3627_*3628delinsGA ENSP00000418548.1:n.*3627_*3628delinsGA
ENST00000461574.1:c.138_139delinsGA
ENST00000468300.5:c.788-655_788-654delinsGA ENSP00000417148.1:n.788-655_788-654delinsGA
ENST00000471181.6:c.3844_3845delinsGA ENSP00000418960.2:p.Glu1282=
ENST00000478531.5:c.785-655_785-654delinsGA ENSP00000420412.1:n.785-655_785-654delinsGA
ENST00000484087.5:c.410-655_410-654delinsGA ENSP00000419481.1:n.410-655_410-654delinsGA
ENST00000487825.5:c.413-655_413-654delinsGA ENSP00000418212.1:n.413-655_413-654delinsGA
ENST00000491747.6:c.788-655_788-654delinsGA ENSP00000420705.2:n.788-655_788-654delinsGA
ENST00000493795.5:c.3703_3704delinsGA ENSP00000418775.1:p.Glu1235=
ENST00000493919.5:c.647-655_647-654delinsGA ENSP00000418819.1:n.647-655_647-654delinsGA
ENST00000586385.5:c.5-27736_5-27735delinsGA ENSP00000465818.1:n.5-27736_5-27735delinsGA
ENST00000591534.5:c.-43-17166_-43-17165delinsGA ENSP00000467329.1:n.-43-17166_-43-17165delinsGA
ENST00000591849.5:c.-99+33584_-99+33585delinsGA ENSP00000465347.1:n.-99+33584_-99+33585delinsGA
NM_007294.3:c.3844_3845delinsGA , LRG_292t1:c.3844_3845delinsGA NP_009225.1:p.Glu1282=
NM_007297.3:c.3703_3704delinsGA NP_009228.2:p.Glu1235=
NM_007298.3:c.788-655_788-654delinsGA NP_009229.2:n.788-655_788-654delinsGA
NM_007299.3:c.788-655_788-654delinsGA NP_009230.2:n.788-655_788-654delinsGA
NM_007300.3:c.3844_3845delinsGA NP_009231.2:p.Glu1282=
NR_027676.1:n.3980_3981delinsGA
NM_007294.4:c.3844_3845delinsGA MANE Select NP_009225.1:p.Glu1282=
NM_007297.4:c.3703_3704delinsGA NP_009228.2:p.Glu1235=
NM_007299.4:c.788-655_788-654delinsGA NP_009230.2:n.788-655_788-654delinsGA
NM_007300.4:c.3844_3845delinsGA NP_009231.2:p.Glu1282=
NR_027676.2:n.4021_4022delinsGA