Canonical Allele Identifier: CA10589782
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 266337
ClinVar RCV Id: RCV000257533
dbSNP Id: rs886040099

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092414_43092417del , CM000679.2:g.43092414_43092417del GRCh38
NC_000017.10:g.41244431_41244434del , CM000679.1:g.41244431_41244434del GRCh37
NC_000017.9:g.38497957_38497960del NCBI36
NG_005905.2:g.125570_125573del , LRG_292:g.125570_125573del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3181_3184del
ENST00000461574.2:c.3117_3120del ENSP00000417241.2:p.Ser1040GlnfsTer7
ENST00000470026.6:c.3117_3120del ENSP00000419274.2:p.Ser1040GlnfsTer7
ENST00000473961.6:c.2991_2994del ENSP00000420201.2:p.Ser998GlnfsTer7
ENST00000476777.6:c.3114_3117del ENSP00000417554.2:p.Ser1039GlnfsTer7
ENST00000477152.6:c.3039_3042del ENSP00000419988.2:p.Ser1014GlnfsTer7
ENST00000478531.6:c.785-1382_785-1379del ENSP00000420412.2:n.785-1382_785-1379del
ENST00000489037.2:c.3039_3042del ENSP00000420781.2:p.Ser1014GlnfsTer7
ENST00000493919.6:c.647-1382_647-1379del ENSP00000418819.2:n.647-1382_647-1379del
ENST00000494123.6:c.3117_3120del ENSP00000419103.2:p.Ser1040GlnfsTer7
ENST00000497488.2:c.2229_2232del ENSP00000418986.2:p.Ser744GlnfsTer7
ENST00000618469.2:c.3117_3120del ENSP00000478114.2:p.Ser1040GlnfsTer7
ENST00000634433.2:c.2994_2997del ENSP00000489431.2:p.Ser999GlnfsTer7
ENST00000644379.2:c.3117_3120del ENSP00000496570.2:p.Ser1040GlnfsTer7
ENST00000644555.2:c.647-1382_647-1379del ENSP00000494614.2:n.647-1382_647-1379del
ENST00000652672.2:c.2976_2979del ENSP00000498906.2:p.Ser993GlnfsTer7
ENST00000484087.6:c.665-1382_665-1379del ENSP00000419481.2:n.665-1382_665-1379del
ENST00000700182.1:c.707-1382_707-1379del ENSP00000514849.1:n.707-1382_707-1379del
ENST00000357654.9:c.3117_3120del MANE Select ENSP00000350283.3:p.Ser1040GlnfsTer7
ENST00000471181.7:c.3117_3120del ENSP00000418960.2:p.Ser1040GlnfsTer7
ENST00000352993.7:c.671-1382_671-1379del ENSP00000312236.5:n.671-1382_671-1379del
ENST00000354071.7:c.3117_3120del ENSP00000326002.7:p.Ser1040GlnfsTer7
ENST00000357654.7:c.3117_3120del ENSP00000350283.3:p.Ser1040GlnfsTer7
ENST00000461221.5:c.*2900_*2903del ENSP00000418548.1:n.*2900_*2903del
ENST00000468300.5:c.788-1382_788-1379del ENSP00000417148.1:n.788-1382_788-1379del
ENST00000471181.6:c.3117_3120del ENSP00000418960.2:p.Ser1040GlnfsTer7
ENST00000478531.5:c.785-1382_785-1379del ENSP00000420412.1:n.785-1382_785-1379del
ENST00000484087.5:c.410-1382_410-1379del ENSP00000419481.1:n.410-1382_410-1379del
ENST00000487825.5:c.413-1382_413-1379del ENSP00000418212.1:n.413-1382_413-1379del
ENST00000491747.6:c.788-1382_788-1379del ENSP00000420705.2:n.788-1382_788-1379del
ENST00000493795.5:c.2976_2979del ENSP00000418775.1:p.Ser993GlnfsTer7
ENST00000493919.5:c.647-1382_647-1379del ENSP00000418819.1:n.647-1382_647-1379del
ENST00000586385.5:c.5-28463_5-28460del ENSP00000465818.1:n.5-28463_5-28460del
ENST00000591534.5:c.-43-17893_-43-17890del ENSP00000467329.1:n.-43-17893_-43-17890del
ENST00000591849.5:c.-99+32857_-99+32860del ENSP00000465347.1:n.-99+32857_-99+32860del
NM_007294.3:c.3117_3120del , LRG_292t1:c.3117_3120del NP_009225.1:p.Ser1040GlnfsTer7
NM_007297.3:c.2976_2979del NP_009228.2:p.Ser993GlnfsTer7
NM_007298.3:c.788-1382_788-1379del NP_009229.2:n.788-1382_788-1379del
NM_007299.3:c.788-1382_788-1379del NP_009230.2:n.788-1382_788-1379del
NM_007300.3:c.3117_3120del NP_009231.2:p.Ser1040GlnfsTer7
NR_027676.1:n.3253_3256del
NM_007294.4:c.3117_3120del MANE Select NP_009225.1:p.Ser1040GlnfsTer7
NM_007297.4:c.2976_2979del NP_009228.2:p.Ser993GlnfsTer7
NM_007299.4:c.788-1382_788-1379del NP_009230.2:n.788-1382_788-1379del
NM_007300.4:c.3117_3120del NP_009231.2:p.Ser1040GlnfsTer7
NR_027676.2:n.3294_3297del