Canonical Allele Identifier: CA10589732

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 266396
• ClinVar RCV Id: RCV000257515
• dbSNP Id: rs886040156
• MyVariant Identifiers: chr17:g.41243914_41243917del (hg19) ; chr17:g.43091897_43091900del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43091897_43091900del , CM000679.2:g.43091897_43091900del	GRCh38
NC_000017.10:g.41243914_41243917del , CM000679.1:g.41243914_41243917del	GRCh37
NC_000017.9:g.38497440_38497443del	NCBI36
NG_005905.2:g.126084_126087del , LRG_292:g.126084_126087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.3695_3698del
ENST00000461574.2:c.3631_3634del	ENSP00000417241.2:p.Ser1211GlnfsTer23
ENST00000470026.6:c.3631_3634del	ENSP00000419274.2:p.Ser1211GlnfsTer23
ENST00000473961.6:c.3505_3508del	ENSP00000420201.2:p.Ser1169GlnfsTer23
ENST00000476777.6:c.3628_3631del	ENSP00000417554.2:p.Ser1210GlnfsTer23
ENST00000477152.6:c.3553_3556del	ENSP00000419988.2:p.Ser1185GlnfsTer23
ENST00000478531.6:c.785-868_785-865del	ENSP00000420412.2:n.785-868_785-865del
ENST00000489037.2:c.3553_3556del	ENSP00000420781.2:p.Ser1185GlnfsTer23
ENST00000493919.6:c.647-868_647-865del	ENSP00000418819.2:n.647-868_647-865del
ENST00000494123.6:c.3631_3634del	ENSP00000419103.2:p.Ser1211GlnfsTer23
ENST00000497488.2:c.2743_2746del	ENSP00000418986.2:p.Ser915GlnfsTer23
ENST00000618469.2:c.3631_3634del	ENSP00000478114.2:p.Ser1211GlnfsTer23
ENST00000634433.2:c.3508_3511del	ENSP00000489431.2:p.Ser1170GlnfsTer23
ENST00000644379.2:c.3631_3634del	ENSP00000496570.2:p.Ser1211GlnfsTer23
ENST00000644555.2:c.647-868_647-865del	ENSP00000494614.2:n.647-868_647-865del
ENST00000652672.2:c.3490_3493del	ENSP00000498906.2:p.Ser1164GlnfsTer23
ENST00000484087.6:c.665-868_665-865del	ENSP00000419481.2:n.665-868_665-865del
ENST00000700182.1:c.707-868_707-865del	ENSP00000514849.1:n.707-868_707-865del
ENST00000357654.9:c.3631_3634del MANE Select	ENSP00000350283.3:p.Ser1211GlnfsTer23
ENST00000471181.7:c.3631_3634del	ENSP00000418960.2:p.Ser1211GlnfsTer23
ENST00000352993.7:c.671-868_671-865del	ENSP00000312236.5:n.671-868_671-865del
ENST00000354071.7:c.3631_3634del	ENSP00000326002.7:p.Ser1211GlnfsTer23
ENST00000357654.7:c.3631_3634del	ENSP00000350283.3:p.Ser1211GlnfsTer23
ENST00000461221.5:c.*3414_*3417del	ENSP00000418548.1:n.*3414_*3417del
ENST00000468300.5:c.788-868_788-865del	ENSP00000417148.1:n.788-868_788-865del
ENST00000471181.6:c.3631_3634del	ENSP00000418960.2:p.Ser1211GlnfsTer23
ENST00000478531.5:c.785-868_785-865del	ENSP00000420412.1:n.785-868_785-865del
ENST00000484087.5:c.410-868_410-865del	ENSP00000419481.1:n.410-868_410-865del
ENST00000487825.5:c.413-868_413-865del	ENSP00000418212.1:n.413-868_413-865del
ENST00000491747.6:c.788-868_788-865del	ENSP00000420705.2:n.788-868_788-865del
ENST00000493795.5:c.3490_3493del	ENSP00000418775.1:p.Ser1164GlnfsTer23
ENST00000493919.5:c.647-868_647-865del	ENSP00000418819.1:n.647-868_647-865del
ENST00000586385.5:c.5-27949_5-27946del	ENSP00000465818.1:n.5-27949_5-27946del
ENST00000591534.5:c.-43-17379_-43-17376del	ENSP00000467329.1:n.-43-17379_-43-17376del
ENST00000591849.5:c.-99+33371_-99+33374del	ENSP00000465347.1:n.-99+33371_-99+33374del
NM_007294.3:c.3631_3634del , LRG_292t1:c.3631_3634del	NP_009225.1:p.Ser1211GlnfsTer23
NM_007297.3:c.3490_3493del	NP_009228.2:p.Ser1164GlnfsTer23
NM_007298.3:c.788-868_788-865del	NP_009229.2:n.788-868_788-865del
NM_007299.3:c.788-868_788-865del	NP_009230.2:n.788-868_788-865del
NM_007300.3:c.3631_3634del	NP_009231.2:p.Ser1211GlnfsTer23
NR_027676.1:n.3767_3770del
NM_007294.4:c.3631_3634del MANE Select	NP_009225.1:p.Ser1211GlnfsTer23
NM_007297.4:c.3490_3493del	NP_009228.2:p.Ser1164GlnfsTer23
NM_007299.4:c.788-868_788-865del	NP_009230.2:n.788-868_788-865del
NM_007300.4:c.3631_3634del	NP_009231.2:p.Ser1211GlnfsTer23
NR_027676.2:n.3808_3811del