Canonical Allele Identifier: CA919844496
Gene: BRCA1 HGNC NCBI

Linked Data

dbSNP Id: rs1567789788

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43091668_43091671del , CM000679.2:g.43091668_43091671del GRCh38
NC_000017.10:g.41243685_41243688del , CM000679.1:g.41243685_41243688del GRCh37
NC_000017.9:g.38497211_38497214del NCBI36
NG_005905.2:g.126314_126317del , LRG_292:g.126314_126317del

Transcript Alleles

HGVS Amino-acid change
ENST00000354071.8:n.3925_3928del
ENST00000461574.2:c.3861_3864del ENSP00000417241.2:p.Glu1288GlnfsTer18
ENST00000470026.6:c.3861_3864del ENSP00000419274.2:p.Glu1288GlnfsTer18
ENST00000473961.6:c.3735_3738del ENSP00000420201.2:p.Glu1246GlnfsTer18
ENST00000476777.6:c.3858_3861del ENSP00000417554.2:p.Glu1287GlnfsTer18
ENST00000477152.6:c.3783_3786del ENSP00000419988.2:p.Glu1262GlnfsTer18
ENST00000478531.6:c.785-638_785-635del ENSP00000420412.2:n.785-638_785-635del
ENST00000489037.2:c.3783_3786del ENSP00000420781.2:p.Glu1262GlnfsTer18
ENST00000493919.6:c.647-638_647-635del ENSP00000418819.2:n.647-638_647-635del
ENST00000494123.6:c.3861_3864del ENSP00000419103.2:p.Glu1288GlnfsTer18
ENST00000497488.2:c.2973_2976del ENSP00000418986.2:p.Glu992GlnfsTer18
ENST00000618469.2:c.3861_3864del ENSP00000478114.2:p.Glu1288GlnfsTer18
ENST00000634433.2:c.3738_3741del ENSP00000489431.2:p.Glu1247GlnfsTer18
ENST00000644379.2:c.3861_3864del ENSP00000496570.2:p.Glu1288GlnfsTer18
ENST00000644555.2:c.647-638_647-635del ENSP00000494614.2:n.647-638_647-635del
ENST00000652672.2:c.3720_3723del ENSP00000498906.2:p.Glu1241GlnfsTer18
ENST00000484087.6:c.665-638_665-635del ENSP00000419481.2:n.665-638_665-635del
ENST00000700182.1:c.707-638_707-635del ENSP00000514849.1:n.707-638_707-635del
ENST00000357654.9:c.3861_3864del MANE Select ENSP00000350283.3:p.Glu1288GlnfsTer18
ENST00000471181.7:c.3861_3864del ENSP00000418960.2:p.Glu1288GlnfsTer18
ENST00000644379.1:c.182_185del
ENST00000352993.7:c.671-638_671-635del ENSP00000312236.5:n.671-638_671-635del
ENST00000354071.7:c.3861_3864del ENSP00000326002.7:p.Glu1288GlnfsTer18
ENST00000357654.7:c.3861_3864del ENSP00000350283.3:p.Glu1288GlnfsTer18
ENST00000461221.5:c.*3644_*3647del ENSP00000418548.1:n.*3644_*3647del
ENST00000461574.1:c.155_158del
ENST00000468300.5:c.788-638_788-635del ENSP00000417148.1:n.788-638_788-635del
ENST00000471181.6:c.3861_3864del ENSP00000418960.2:p.Glu1288GlnfsTer18
ENST00000478531.5:c.785-638_785-635del ENSP00000420412.1:n.785-638_785-635del
ENST00000484087.5:c.410-638_410-635del ENSP00000419481.1:n.410-638_410-635del
ENST00000487825.5:c.413-638_413-635del ENSP00000418212.1:n.413-638_413-635del
ENST00000491747.6:c.788-638_788-635del ENSP00000420705.2:n.788-638_788-635del
ENST00000493795.5:c.3720_3723del ENSP00000418775.1:p.Glu1241GlnfsTer18
ENST00000493919.5:c.647-638_647-635del ENSP00000418819.1:n.647-638_647-635del
ENST00000586385.5:c.5-27719_5-27716del ENSP00000465818.1:n.5-27719_5-27716del
ENST00000591534.5:c.-43-17149_-43-17146del ENSP00000467329.1:n.-43-17149_-43-17146de...
ENST00000591849.5:c.-99+33601_-99+33604del ENSP00000465347.1:n.-99+33601_-99+33604de...
NM_007294.3:c.3861_3864del , LRG_292t1:c.3861_3864del NP_009225.1:p.Glu1288GlnfsTer18
NM_007297.3:c.3720_3723del NP_009228.2:p.Glu1241GlnfsTer18
NM_007298.3:c.788-638_788-635del NP_009229.2:n.788-638_788-635del
NM_007299.3:c.788-638_788-635del NP_009230.2:n.788-638_788-635del
NM_007300.3:c.3861_3864del NP_009231.2:p.Glu1288GlnfsTer18
NR_027676.1:n.3997_4000del
NM_007294.4:c.3861_3864del MANE Select NP_009225.1:p.Glu1288GlnfsTer18
NM_007297.4:c.3720_3723del NP_009228.2:p.Glu1241GlnfsTer18
NM_007299.4:c.788-638_788-635del NP_009230.2:n.788-638_788-635del
NM_007300.4:c.3861_3864del NP_009231.2:p.Glu1288GlnfsTer18
NR_027676.2:n.4038_4041del