Canonical Allele Identifier: CA001971
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 54749
dbSNP Id: rs80357749

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092512_43092515del , CM000679.2:g.43092512_43092515del GRCh38
NC_000017.10:g.41244529_41244532del , CM000679.1:g.41244529_41244532del GRCh37
NC_000017.9:g.38498055_38498058del NCBI36
NG_005905.2:g.125471_125474del , LRG_292:g.125471_125474del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3082_3085del
ENST00000461574.2:c.3018_3021del ENSP00000417241.2:p.His1006GlnfsTer17
ENST00000470026.6:c.3018_3021del ENSP00000419274.2:p.His1006GlnfsTer17
ENST00000473961.6:c.2892_2895del ENSP00000420201.2:p.His964GlnfsTer17
ENST00000476777.6:c.3015_3018del ENSP00000417554.2:p.His1005GlnfsTer17
ENST00000477152.6:c.2940_2943del ENSP00000419988.2:p.His980GlnfsTer17
ENST00000478531.6:c.785-1481_785-1478del ENSP00000420412.2:n.785-1481_785-1478del
ENST00000489037.2:c.2940_2943del ENSP00000420781.2:p.His980GlnfsTer17
ENST00000493919.6:c.647-1481_647-1478del ENSP00000418819.2:n.647-1481_647-1478del
ENST00000494123.6:c.3018_3021del ENSP00000419103.2:p.His1006GlnfsTer17
ENST00000497488.2:c.2130_2133del ENSP00000418986.2:p.His710GlnfsTer17
ENST00000618469.2:c.3018_3021del ENSP00000478114.2:p.His1006GlnfsTer17
ENST00000634433.2:c.2895_2898del ENSP00000489431.2:p.His965GlnfsTer17
ENST00000644379.2:c.3018_3021del ENSP00000496570.2:p.His1006GlnfsTer17
ENST00000644555.2:c.647-1481_647-1478del ENSP00000494614.2:n.647-1481_647-1478del
ENST00000652672.2:c.2877_2880del ENSP00000498906.2:p.His959GlnfsTer17
ENST00000484087.6:c.665-1481_665-1478del ENSP00000419481.2:n.665-1481_665-1478del
ENST00000700182.1:c.707-1481_707-1478del ENSP00000514849.1:n.707-1481_707-1478del
ENST00000357654.9:c.3018_3021del MANE Select ENSP00000350283.3:p.His1006GlnfsTer17
ENST00000471181.7:c.3018_3021del ENSP00000418960.2:p.His1006GlnfsTer17
ENST00000352993.7:c.671-1481_671-1478del ENSP00000312236.5:n.671-1481_671-1478del
ENST00000354071.7:c.3018_3021del ENSP00000326002.7:p.His1006GlnfsTer17
ENST00000357654.7:c.3018_3021del ENSP00000350283.3:p.His1006GlnfsTer17
ENST00000461221.5:c.*2801_*2804del ENSP00000418548.1:n.*2801_*2804del
ENST00000468300.5:c.788-1481_788-1478del ENSP00000417148.1:n.788-1481_788-1478del
ENST00000471181.6:c.3018_3021del ENSP00000418960.2:p.His1006GlnfsTer17
ENST00000478531.5:c.785-1481_785-1478del ENSP00000420412.1:n.785-1481_785-1478del
ENST00000484087.5:c.410-1481_410-1478del ENSP00000419481.1:n.410-1481_410-1478del
ENST00000487825.5:c.413-1481_413-1478del ENSP00000418212.1:n.413-1481_413-1478del
ENST00000491747.6:c.788-1481_788-1478del ENSP00000420705.2:n.788-1481_788-1478del
ENST00000493795.5:c.2877_2880del ENSP00000418775.1:p.His959GlnfsTer17
ENST00000493919.5:c.647-1481_647-1478del ENSP00000418819.1:n.647-1481_647-1478del
ENST00000586385.5:c.5-28562_5-28559del ENSP00000465818.1:n.5-28562_5-28559del
ENST00000591534.5:c.-43-17992_-43-17989del ENSP00000467329.1:n.-43-17992_-43-17989del
ENST00000591849.5:c.-99+32758_-99+32761del ENSP00000465347.1:n.-99+32758_-99+32761del
NM_007294.3:c.3018_3021del , LRG_292t1:c.3018_3021del NP_009225.1:p.His1006GlnfsTer17
NM_007297.3:c.2877_2880del NP_009228.2:p.His959GlnfsTer17
NM_007298.3:c.788-1481_788-1478del NP_009229.2:n.788-1481_788-1478del
NM_007299.3:c.788-1481_788-1478del NP_009230.2:n.788-1481_788-1478del
NM_007300.3:c.3018_3021del NP_009231.2:p.His1006GlnfsTer17
NR_027676.1:n.3154_3157del
NM_007294.4:c.3018_3021del MANE Select NP_009225.1:p.His1006GlnfsTer17
NM_007297.4:c.2877_2880del NP_009228.2:p.His959GlnfsTer17
NM_007299.4:c.788-1481_788-1478del NP_009230.2:n.788-1481_788-1478del
NM_007300.4:c.3018_3021del NP_009231.2:p.His1006GlnfsTer17
NR_027676.2:n.3195_3198del