Canonical Allele Identifier: CA2260783020
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092525_43092526delinsGT , CM000679.2:g.43092525_43092526delinsGT GRCh38
NC_000017.10:g.41244542_41244543delinsGT , CM000679.1:g.41244542_41244543delinsGT GRCh37
NC_000017.9:g.38498068_38498069delinsGT NCBI36
NG_005905.2:g.125458_125459delinsAC , LRG_292:g.125458_125459delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3069_3070delinsAC
ENST00000461574.2:c.3005_3006delinsAC ENSP00000417241.2:p.Asn1002=
ENST00000470026.6:c.3005_3006delinsAC ENSP00000419274.2:p.Asn1002=
ENST00000473961.6:c.2879_2880delinsAC ENSP00000420201.2:p.Asn960=
ENST00000476777.6:c.3002_3003delinsAC ENSP00000417554.2:p.Asn1001=
ENST00000477152.6:c.2927_2928delinsAC ENSP00000419988.2:p.Asn976=
ENST00000478531.6:c.785-1494_785-1493delinsAC ENSP00000420412.2:n.785-1494_785-1493delinsAC
ENST00000489037.2:c.2927_2928delinsAC ENSP00000420781.2:p.Asn976=
ENST00000493919.6:c.647-1494_647-1493delinsAC ENSP00000418819.2:n.647-1494_647-1493delinsAC
ENST00000494123.6:c.3005_3006delinsAC ENSP00000419103.2:p.Asn1002=
ENST00000497488.2:c.2117_2118delinsAC ENSP00000418986.2:p.Asn706=
ENST00000618469.2:c.3005_3006delinsAC ENSP00000478114.2:p.Asn1002=
ENST00000634433.2:c.2882_2883delinsAC ENSP00000489431.2:p.Asn961=
ENST00000644379.2:c.3005_3006delinsAC ENSP00000496570.2:p.Asn1002=
ENST00000644555.2:c.647-1494_647-1493delinsAC ENSP00000494614.2:n.647-1494_647-1493delinsAC
ENST00000652672.2:c.2864_2865delinsAC ENSP00000498906.2:p.Asn955=
ENST00000484087.6:c.665-1494_665-1493delinsAC ENSP00000419481.2:n.665-1494_665-1493delinsAC
ENST00000700182.1:c.707-1494_707-1493delinsAC ENSP00000514849.1:n.707-1494_707-1493delinsAC
ENST00000357654.9:c.3005_3006delinsAC MANE Select ENSP00000350283.3:p.Asn1002=
ENST00000471181.7:c.3005_3006delinsAC ENSP00000418960.2:p.Asn1002=
ENST00000352993.7:c.671-1494_671-1493delinsAC ENSP00000312236.5:n.671-1494_671-1493delinsAC
ENST00000354071.7:c.3005_3006delinsAC ENSP00000326002.7:p.Asn1002=
ENST00000357654.7:c.3005_3006delinsAC ENSP00000350283.3:p.Asn1002=
ENST00000461221.5:c.*2788_*2789delinsAC ENSP00000418548.1:n.*2788_*2789delinsAC
ENST00000468300.5:c.788-1494_788-1493delinsAC ENSP00000417148.1:n.788-1494_788-1493delinsAC
ENST00000471181.6:c.3005_3006delinsAC ENSP00000418960.2:p.Asn1002=
ENST00000478531.5:c.785-1494_785-1493delinsAC ENSP00000420412.1:n.785-1494_785-1493delinsAC
ENST00000484087.5:c.410-1494_410-1493delinsAC ENSP00000419481.1:n.410-1494_410-1493delinsAC
ENST00000487825.5:c.413-1494_413-1493delinsAC ENSP00000418212.1:n.413-1494_413-1493delinsAC
ENST00000491747.6:c.788-1494_788-1493delinsAC ENSP00000420705.2:n.788-1494_788-1493delinsAC
ENST00000493795.5:c.2864_2865delinsAC ENSP00000418775.1:p.Asn955=
ENST00000493919.5:c.647-1494_647-1493delinsAC ENSP00000418819.1:n.647-1494_647-1493delinsAC
ENST00000586385.5:c.5-28575_5-28574delinsAC ENSP00000465818.1:n.5-28575_5-28574delinsAC
ENST00000591534.5:c.-43-18005_-43-18004delinsAC ENSP00000467329.1:n.-43-18005_-43-18004delinsAC
ENST00000591849.5:c.-99+32745_-99+32746delinsAC ENSP00000465347.1:n.-99+32745_-99+32746delinsAC
NM_007294.3:c.3005_3006delinsAC , LRG_292t1:c.3005_3006delinsAC NP_009225.1:p.Asn1002=
NM_007297.3:c.2864_2865delinsAC NP_009228.2:p.Asn955=
NM_007298.3:c.788-1494_788-1493delinsAC NP_009229.2:n.788-1494_788-1493delinsAC
NM_007299.3:c.788-1494_788-1493delinsAC NP_009230.2:n.788-1494_788-1493delinsAC
NM_007300.3:c.3005_3006delinsAC NP_009231.2:p.Asn1002=
NR_027676.1:n.3141_3142delinsAC
NM_007294.4:c.3005_3006delinsAC MANE Select NP_009225.1:p.Asn1002=
NM_007297.4:c.2864_2865delinsAC NP_009228.2:p.Asn955=
NM_007299.4:c.788-1494_788-1493delinsAC NP_009230.2:n.788-1494_788-1493delinsAC
NM_007300.4:c.3005_3006delinsAC NP_009231.2:p.Asn1002=
NR_027676.2:n.3182_3183delinsAC