Canonical Allele Identifier: CA2260782773
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092268_43092269delinsAC , CM000679.2:g.43092268_43092269delinsAC GRCh38
NC_000017.10:g.41244285_41244286delinsAC , CM000679.1:g.41244285_41244286delinsAC GRCh37
NC_000017.9:g.38497811_38497812delinsAC NCBI36
NG_005905.2:g.125715_125716delinsGT , LRG_292:g.125715_125716delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3326_3327delinsGT
ENST00000461574.2:c.3262_3263delinsGT ENSP00000417241.2:p.Val1088=
ENST00000470026.6:c.3262_3263delinsGT ENSP00000419274.2:p.Val1088=
ENST00000473961.6:c.3136_3137delinsGT ENSP00000420201.2:p.Val1046=
ENST00000476777.6:c.3259_3260delinsGT ENSP00000417554.2:p.Val1087=
ENST00000477152.6:c.3184_3185delinsGT ENSP00000419988.2:p.Val1062=
ENST00000478531.6:c.785-1237_785-1236delinsGT ENSP00000420412.2:n.785-1237_785-1236delinsGT
ENST00000489037.2:c.3184_3185delinsGT ENSP00000420781.2:p.Val1062=
ENST00000493919.6:c.647-1237_647-1236delinsGT ENSP00000418819.2:n.647-1237_647-1236delinsGT
ENST00000494123.6:c.3262_3263delinsGT ENSP00000419103.2:p.Val1088=
ENST00000497488.2:c.2374_2375delinsGT ENSP00000418986.2:p.Val792=
ENST00000618469.2:c.3262_3263delinsGT ENSP00000478114.2:p.Val1088=
ENST00000634433.2:c.3139_3140delinsGT ENSP00000489431.2:p.Val1047=
ENST00000644379.2:c.3262_3263delinsGT ENSP00000496570.2:p.Val1088=
ENST00000644555.2:c.647-1237_647-1236delinsGT ENSP00000494614.2:n.647-1237_647-1236delinsGT
ENST00000652672.2:c.3121_3122delinsGT ENSP00000498906.2:p.Val1041=
ENST00000484087.6:c.665-1237_665-1236delinsGT ENSP00000419481.2:n.665-1237_665-1236delinsGT
ENST00000700182.1:c.707-1237_707-1236delinsGT ENSP00000514849.1:n.707-1237_707-1236delinsGT
ENST00000357654.9:c.3262_3263delinsGT MANE Select ENSP00000350283.3:p.Val1088=
ENST00000471181.7:c.3262_3263delinsGT ENSP00000418960.2:p.Val1088=
ENST00000352993.7:c.671-1237_671-1236delinsGT ENSP00000312236.5:n.671-1237_671-1236delinsGT
ENST00000354071.7:c.3262_3263delinsGT ENSP00000326002.7:p.Val1088=
ENST00000357654.7:c.3262_3263delinsGT ENSP00000350283.3:p.Val1088=
ENST00000461221.5:c.*3045_*3046delinsGT ENSP00000418548.1:n.*3045_*3046delinsGT
ENST00000468300.5:c.788-1237_788-1236delinsGT ENSP00000417148.1:n.788-1237_788-1236delinsGT
ENST00000471181.6:c.3262_3263delinsGT ENSP00000418960.2:p.Val1088=
ENST00000478531.5:c.785-1237_785-1236delinsGT ENSP00000420412.1:n.785-1237_785-1236delinsGT
ENST00000484087.5:c.410-1237_410-1236delinsGT ENSP00000419481.1:n.410-1237_410-1236delinsGT
ENST00000487825.5:c.413-1237_413-1236delinsGT ENSP00000418212.1:n.413-1237_413-1236delinsGT
ENST00000491747.6:c.788-1237_788-1236delinsGT ENSP00000420705.2:n.788-1237_788-1236delinsGT
ENST00000493795.5:c.3121_3122delinsGT ENSP00000418775.1:p.Val1041=
ENST00000493919.5:c.647-1237_647-1236delinsGT ENSP00000418819.1:n.647-1237_647-1236delinsGT
ENST00000586385.5:c.5-28318_5-28317delinsGT ENSP00000465818.1:n.5-28318_5-28317delinsGT
ENST00000591534.5:c.-43-17748_-43-17747delinsGT ENSP00000467329.1:n.-43-17748_-43-17747delinsGT
ENST00000591849.5:c.-99+33002_-99+33003delinsGT ENSP00000465347.1:n.-99+33002_-99+33003delinsGT
NM_007294.3:c.3262_3263delinsGT , LRG_292t1:c.3262_3263delinsGT NP_009225.1:p.Val1088=
NM_007297.3:c.3121_3122delinsGT NP_009228.2:p.Val1041=
NM_007298.3:c.788-1237_788-1236delinsGT NP_009229.2:n.788-1237_788-1236delinsGT
NM_007299.3:c.788-1237_788-1236delinsGT NP_009230.2:n.788-1237_788-1236delinsGT
NM_007300.3:c.3262_3263delinsGT NP_009231.2:p.Val1088=
NR_027676.1:n.3398_3399delinsGT
NM_007294.4:c.3262_3263delinsGT MANE Select NP_009225.1:p.Val1088=
NM_007297.4:c.3121_3122delinsGT NP_009228.2:p.Val1041=
NM_007299.4:c.788-1237_788-1236delinsGT NP_009230.2:n.788-1237_788-1236delinsGT
NM_007300.4:c.3262_3263delinsGT NP_009231.2:p.Val1088=
NR_027676.2:n.3439_3440delinsGT