Canonical Allele Identifier: CA001949
Gene: BRCA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 54743
dbSNP Id: rs80358333

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43092529_43092534del , CM000679.2:g.43092529_43092534del GRCh38
NC_000017.10:g.41244546_41244551del , CM000679.1:g.41244546_41244551del GRCh37
NC_000017.9:g.38498072_38498077del NCBI36
NG_005905.2:g.125451_125456del , LRG_292:g.125451_125456del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.3062_3067del
ENST00000461574.2:c.2998_3003del ENSP00000417241.2:p.Glu1000_Glu1001del
ENST00000470026.6:c.2998_3003del ENSP00000419274.2:p.Glu1000_Glu1001del
ENST00000473961.6:c.2872_2877del ENSP00000420201.2:p.Glu958_Glu959del
ENST00000476777.6:c.2995_3000del ENSP00000417554.2:p.Glu999_Glu1000del
ENST00000477152.6:c.2920_2925del ENSP00000419988.2:p.Glu974_Glu975del
ENST00000478531.6:c.785-1501_785-1496del ENSP00000420412.2:n.785-1501_785-1496del
ENST00000489037.2:c.2920_2925del ENSP00000420781.2:p.Glu974_Glu975del
ENST00000493919.6:c.647-1501_647-1496del ENSP00000418819.2:n.647-1501_647-1496del
ENST00000494123.6:c.2998_3003del ENSP00000419103.2:p.Glu1000_Glu1001del
ENST00000497488.2:c.2110_2115del ENSP00000418986.2:p.Glu704_Glu705del
ENST00000618469.2:c.2998_3003del ENSP00000478114.2:p.Glu1000_Glu1001del
ENST00000634433.2:c.2875_2880del ENSP00000489431.2:p.Glu959_Glu960del
ENST00000644379.2:c.2998_3003del ENSP00000496570.2:p.Glu1000_Glu1001del
ENST00000644555.2:c.647-1501_647-1496del ENSP00000494614.2:n.647-1501_647-1496del
ENST00000652672.2:c.2857_2862del ENSP00000498906.2:p.Glu953_Glu954del
ENST00000484087.6:c.665-1501_665-1496del ENSP00000419481.2:n.665-1501_665-1496del
ENST00000700182.1:c.707-1501_707-1496del ENSP00000514849.1:n.707-1501_707-1496del
ENST00000357654.9:c.2998_3003del MANE Select ENSP00000350283.3:p.Glu1000_Glu1001del
ENST00000471181.7:c.2998_3003del ENSP00000418960.2:p.Glu1000_Glu1001del
ENST00000352993.7:c.671-1501_671-1496del ENSP00000312236.5:n.671-1501_671-1496del
ENST00000354071.7:c.2998_3003del ENSP00000326002.7:p.Glu1000_Glu1001del
ENST00000357654.7:c.2998_3003del ENSP00000350283.3:p.Glu1000_Glu1001del
ENST00000461221.5:c.*2781_*2786del ENSP00000418548.1:n.*2781_*2786del
ENST00000468300.5:c.788-1501_788-1496del ENSP00000417148.1:n.788-1501_788-1496del
ENST00000471181.6:c.2998_3003del ENSP00000418960.2:p.Glu1000_Glu1001del
ENST00000478531.5:c.785-1501_785-1496del ENSP00000420412.1:n.785-1501_785-1496del
ENST00000484087.5:c.410-1501_410-1496del ENSP00000419481.1:n.410-1501_410-1496del
ENST00000487825.5:c.413-1501_413-1496del ENSP00000418212.1:n.413-1501_413-1496del
ENST00000491747.6:c.788-1501_788-1496del ENSP00000420705.2:n.788-1501_788-1496del
ENST00000493795.5:c.2857_2862del ENSP00000418775.1:p.Glu953_Glu954del
ENST00000493919.5:c.647-1501_647-1496del ENSP00000418819.1:n.647-1501_647-1496del
ENST00000586385.5:c.5-28582_5-28577del ENSP00000465818.1:n.5-28582_5-28577del
ENST00000591534.5:c.-43-18012_-43-18007del ENSP00000467329.1:n.-43-18012_-43-18007del
ENST00000591849.5:c.-99+32738_-99+32743del ENSP00000465347.1:n.-99+32738_-99+32743del
NM_007294.3:c.2998_3003del , LRG_292t1:c.2998_3003del NP_009225.1:p.Glu1000_Glu1001del
NM_007297.3:c.2857_2862del NP_009228.2:p.Glu953_Glu954del
NM_007298.3:c.788-1501_788-1496del NP_009229.2:n.788-1501_788-1496del
NM_007299.3:c.788-1501_788-1496del NP_009230.2:n.788-1501_788-1496del
NM_007300.3:c.2998_3003del NP_009231.2:p.Glu1000_Glu1001del
NR_027676.1:n.3134_3139del
NM_007294.4:c.2998_3003del MANE Select NP_009225.1:p.Glu1000_Glu1001del
NM_007297.4:c.2857_2862del NP_009228.2:p.Glu953_Glu954del
NM_007299.4:c.788-1501_788-1496del NP_009230.2:n.788-1501_788-1496del
NM_007300.4:c.2998_3003del NP_009231.2:p.Glu1000_Glu1001del
NR_027676.2:n.3175_3180del