Canonical Allele Identifier: CA2580093911
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1801653
ClinVar RCV Id: RCV003164689

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092432_43092433del , CM000679.2:g.43092432_43092433del GRCh38
NC_000017.10:g.41244449_41244450del , CM000679.1:g.41244449_41244450del GRCh37
NC_000017.9:g.38497975_38497976del NCBI36
NG_005905.2:g.125553_125554del , LRG_292:g.125553_125554del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3164_3165del
ENST00000461574.2:c.3100_3101del ENSP00000417241.2:p.Asn1034CysfsTer3
ENST00000470026.6:c.3100_3101del ENSP00000419274.2:p.Asn1034CysfsTer3
ENST00000473961.6:c.2974_2975del ENSP00000420201.2:p.Asn992CysfsTer3
ENST00000476777.6:c.3097_3098del ENSP00000417554.2:p.Asn1033CysfsTer3
ENST00000477152.6:c.3022_3023del ENSP00000419988.2:p.Asn1008CysfsTer3
ENST00000478531.6:c.785-1399_785-1398del ENSP00000420412.2:n.785-1399_785-1398del
ENST00000489037.2:c.3022_3023del ENSP00000420781.2:p.Asn1008CysfsTer3
ENST00000493919.6:c.647-1399_647-1398del ENSP00000418819.2:n.647-1399_647-1398del
ENST00000494123.6:c.3100_3101del ENSP00000419103.2:p.Asn1034CysfsTer3
ENST00000497488.2:c.2212_2213del ENSP00000418986.2:p.Asn738CysfsTer3
ENST00000618469.2:c.3100_3101del ENSP00000478114.2:p.Asn1034CysfsTer3
ENST00000634433.2:c.2977_2978del ENSP00000489431.2:p.Asn993CysfsTer3
ENST00000644379.2:c.3100_3101del ENSP00000496570.2:p.Asn1034CysfsTer3
ENST00000644555.2:c.647-1399_647-1398del ENSP00000494614.2:n.647-1399_647-1398del
ENST00000652672.2:c.2959_2960del ENSP00000498906.2:p.Asn987CysfsTer3
ENST00000484087.6:c.665-1399_665-1398del ENSP00000419481.2:n.665-1399_665-1398del
ENST00000700182.1:c.707-1399_707-1398del ENSP00000514849.1:n.707-1399_707-1398del
ENST00000357654.9:c.3100_3101del MANE Select ENSP00000350283.3:p.Asn1034CysfsTer3
ENST00000471181.7:c.3100_3101del ENSP00000418960.2:p.Asn1034CysfsTer3
ENST00000352993.7:c.671-1399_671-1398del ENSP00000312236.5:n.671-1399_671-1398del
ENST00000354071.7:c.3100_3101del ENSP00000326002.7:p.Asn1034CysfsTer3
ENST00000357654.7:c.3100_3101del ENSP00000350283.3:p.Asn1034CysfsTer3
ENST00000461221.5:c.*2883_*2884del ENSP00000418548.1:n.*2883_*2884del
ENST00000468300.5:c.788-1399_788-1398del ENSP00000417148.1:n.788-1399_788-1398del
ENST00000471181.6:c.3100_3101del ENSP00000418960.2:p.Asn1034CysfsTer3
ENST00000478531.5:c.785-1399_785-1398del ENSP00000420412.1:n.785-1399_785-1398del
ENST00000484087.5:c.410-1399_410-1398del ENSP00000419481.1:n.410-1399_410-1398del
ENST00000487825.5:c.413-1399_413-1398del ENSP00000418212.1:n.413-1399_413-1398del
ENST00000491747.6:c.788-1399_788-1398del ENSP00000420705.2:n.788-1399_788-1398del
ENST00000493795.5:c.2959_2960del ENSP00000418775.1:p.Asn987CysfsTer3
ENST00000493919.5:c.647-1399_647-1398del ENSP00000418819.1:n.647-1399_647-1398del
ENST00000586385.5:c.5-28480_5-28479del ENSP00000465818.1:n.5-28480_5-28479del
ENST00000591534.5:c.-43-17910_-43-17909del ENSP00000467329.1:n.-43-17910_-43-17909del
ENST00000591849.5:c.-99+32840_-99+32841del ENSP00000465347.1:n.-99+32840_-99+32841del
NM_007294.3:c.3100_3101del , LRG_292t1:c.3100_3101del NP_009225.1:p.Asn1034CysfsTer3
NM_007297.3:c.2959_2960del NP_009228.2:p.Asn987CysfsTer3
NM_007298.3:c.788-1399_788-1398del NP_009229.2:n.788-1399_788-1398del
NM_007299.3:c.788-1399_788-1398del NP_009230.2:n.788-1399_788-1398del
NM_007300.3:c.3100_3101del NP_009231.2:p.Asn1034CysfsTer3
NR_027676.1:n.3236_3237del
NM_007294.4:c.3100_3101del MANE Select NP_009225.1:p.Asn1034CysfsTer3
NM_007297.4:c.2959_2960del NP_009228.2:p.Asn987CysfsTer3
NM_007299.4:c.788-1399_788-1398del NP_009230.2:n.788-1399_788-1398del
NM_007300.4:c.3100_3101del NP_009231.2:p.Asn1034CysfsTer3
NR_027676.2:n.3277_3278del