Canonical Allele Identifier: CA2260782922
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092416_43092417delinsCT , CM000679.2:g.43092416_43092417delinsCT GRCh38
NC_000017.10:g.41244433_41244434delinsCT , CM000679.1:g.41244433_41244434delinsCT GRCh37
NC_000017.9:g.38497959_38497960delinsCT NCBI36
NG_005905.2:g.125567_125568delinsAG , LRG_292:g.125567_125568delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3178_3179delinsAG
ENST00000461574.2:c.3114_3115delinsAG ENSP00000417241.2:p.Glu1038=
ENST00000470026.6:c.3114_3115delinsAG ENSP00000419274.2:p.Glu1038=
ENST00000473961.6:c.2988_2989delinsAG ENSP00000420201.2:p.Glu996=
ENST00000476777.6:c.3111_3112delinsAG ENSP00000417554.2:p.Glu1037=
ENST00000477152.6:c.3036_3037delinsAG ENSP00000419988.2:p.Glu1012=
ENST00000478531.6:c.785-1385_785-1384delinsAG ENSP00000420412.2:n.785-1385_785-1384delinsAG
ENST00000489037.2:c.3036_3037delinsAG ENSP00000420781.2:p.Glu1012=
ENST00000493919.6:c.647-1385_647-1384delinsAG ENSP00000418819.2:n.647-1385_647-1384delinsAG
ENST00000494123.6:c.3114_3115delinsAG ENSP00000419103.2:p.Glu1038=
ENST00000497488.2:c.2226_2227delinsAG ENSP00000418986.2:p.Glu742=
ENST00000618469.2:c.3114_3115delinsAG ENSP00000478114.2:p.Glu1038=
ENST00000634433.2:c.2991_2992delinsAG ENSP00000489431.2:p.Glu997=
ENST00000644379.2:c.3114_3115delinsAG ENSP00000496570.2:p.Glu1038=
ENST00000644555.2:c.647-1385_647-1384delinsAG ENSP00000494614.2:n.647-1385_647-1384delinsAG
ENST00000652672.2:c.2973_2974delinsAG ENSP00000498906.2:p.Glu991=
ENST00000484087.6:c.665-1385_665-1384delinsAG ENSP00000419481.2:n.665-1385_665-1384delinsAG
ENST00000700182.1:c.707-1385_707-1384delinsAG ENSP00000514849.1:n.707-1385_707-1384delinsAG
ENST00000357654.9:c.3114_3115delinsAG MANE Select ENSP00000350283.3:p.Glu1038=
ENST00000471181.7:c.3114_3115delinsAG ENSP00000418960.2:p.Glu1038=
ENST00000352993.7:c.671-1385_671-1384delinsAG ENSP00000312236.5:n.671-1385_671-1384delinsAG
ENST00000354071.7:c.3114_3115delinsAG ENSP00000326002.7:p.Glu1038=
ENST00000357654.7:c.3114_3115delinsAG ENSP00000350283.3:p.Glu1038=
ENST00000461221.5:c.*2897_*2898delinsAG ENSP00000418548.1:n.*2897_*2898delinsAG
ENST00000468300.5:c.788-1385_788-1384delinsAG ENSP00000417148.1:n.788-1385_788-1384delinsAG
ENST00000471181.6:c.3114_3115delinsAG ENSP00000418960.2:p.Glu1038=
ENST00000478531.5:c.785-1385_785-1384delinsAG ENSP00000420412.1:n.785-1385_785-1384delinsAG
ENST00000484087.5:c.410-1385_410-1384delinsAG ENSP00000419481.1:n.410-1385_410-1384delinsAG
ENST00000487825.5:c.413-1385_413-1384delinsAG ENSP00000418212.1:n.413-1385_413-1384delinsAG
ENST00000491747.6:c.788-1385_788-1384delinsAG ENSP00000420705.2:n.788-1385_788-1384delinsAG
ENST00000493795.5:c.2973_2974delinsAG ENSP00000418775.1:p.Glu991=
ENST00000493919.5:c.647-1385_647-1384delinsAG ENSP00000418819.1:n.647-1385_647-1384delinsAG
ENST00000586385.5:c.5-28466_5-28465delinsAG ENSP00000465818.1:n.5-28466_5-28465delinsAG
ENST00000591534.5:c.-43-17896_-43-17895delinsAG ENSP00000467329.1:n.-43-17896_-43-17895delinsAG
ENST00000591849.5:c.-99+32854_-99+32855delinsAG ENSP00000465347.1:n.-99+32854_-99+32855delinsAG
NM_007294.3:c.3114_3115delinsAG , LRG_292t1:c.3114_3115delinsAG NP_009225.1:p.Glu1038=
NM_007297.3:c.2973_2974delinsAG NP_009228.2:p.Glu991=
NM_007298.3:c.788-1385_788-1384delinsAG NP_009229.2:n.788-1385_788-1384delinsAG
NM_007299.3:c.788-1385_788-1384delinsAG NP_009230.2:n.788-1385_788-1384delinsAG
NM_007300.3:c.3114_3115delinsAG NP_009231.2:p.Glu1038=
NR_027676.1:n.3250_3251delinsAG
NM_007294.4:c.3114_3115delinsAG MANE Select NP_009225.1:p.Glu1038=
NM_007297.4:c.2973_2974delinsAG NP_009228.2:p.Glu991=
NM_007299.4:c.788-1385_788-1384delinsAG NP_009230.2:n.788-1385_788-1384delinsAG
NM_007300.4:c.3114_3115delinsAG NP_009231.2:p.Glu1038=
NR_027676.2:n.3291_3292delinsAG