Canonical Allele Identifier: CA658824551

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 548826
• ClinVar RCV Id: RCV001855407
• dbSNP Id: rs1555592956
• MyVariant Identifiers: chr17:g.41246679del (hg19) ; chr17:g.43094662del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43094664del , CM000679.2:g.43094664del	GRCh38
NC_000017.10:g.41246681del , CM000679.1:g.41246681del	GRCh37
NC_000017.9:g.38500207del	NCBI36
NG_005905.2:g.123322del , LRG_292:g.123322del

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.933del
ENST00000461574.2:c.869del	ENSP00000417241.2:p.Leu290TyrfsTer8
ENST00000470026.6:c.869del	ENSP00000419274.2:p.Leu290TyrfsTer8
ENST00000473961.6:c.743del	ENSP00000420201.2:p.Leu248TyrfsTer8
ENST00000476777.6:c.866del	ENSP00000417554.2:p.Leu289TyrfsTer8
ENST00000477152.6:c.791del	ENSP00000419988.2:p.Leu264TyrfsTer8
ENST00000478531.6:c.784+82del	ENSP00000420412.2:n.784+82del
ENST00000489037.2:c.791del	ENSP00000420781.2:p.Leu264TyrfsTer8
ENST00000493919.6:c.646+82del	ENSP00000418819.2:n.646+82del
ENST00000494123.6:c.869del	ENSP00000419103.2:p.Leu290TyrfsTer8
ENST00000497488.2:c.-20del	ENSP00000418986.2:n.-20del
ENST00000618469.2:c.869del	ENSP00000478114.2:p.Leu290TyrfsTer8
ENST00000634433.2:c.746del	ENSP00000489431.2:p.Leu249TyrfsTer8
ENST00000644379.2:c.869del	ENSP00000496570.2:p.Leu290TyrfsTer8
ENST00000644555.2:c.646+82del	ENSP00000494614.2:n.646+82del
ENST00000652672.2:c.728del	ENSP00000498906.2:p.Leu243TyrfsTer8
ENST00000484087.6:c.664+82del	ENSP00000419481.2:n.664+82del
ENST00000700182.1:c.706+82del	ENSP00000514849.1:n.706+82del
ENST00000700183.1:c.*877del	ENSP00000514850.1:n.*877del
ENST00000357654.9:c.869del MANE Select	ENSP00000350283.3:p.Leu290TyrfsTer8
ENST00000471181.7:c.869del	ENSP00000418960.2:p.Leu290TyrfsTer8
ENST00000642945.1:c.*743del	ENSP00000495897.1:n.*743del
ENST00000652672.1:c.728del	ENSP00000498906.1:p.Leu243TyrfsTer8
ENST00000352993.7:c.670+1184del	ENSP00000312236.5:n.670+1184del
ENST00000354071.7:c.869del	ENSP00000326002.7:p.Leu290TyrfsTer8
ENST00000357654.7:c.869del	ENSP00000350283.3:p.Leu290TyrfsTer8
ENST00000412061.3:c.220del
ENST00000461221.5:c.*652del	ENSP00000418548.1:n.*652del
ENST00000468300.5:c.787+82del	ENSP00000417148.1:n.787+82del
ENST00000470026.5:c.869del	ENSP00000419274.1:p.Leu290TyrfsTer8
ENST00000471181.6:c.869del	ENSP00000418960.2:p.Leu290TyrfsTer8
ENST00000473961.5:c.466del
ENST00000477152.5:c.791del	ENSP00000419988.1:p.Leu264TyrfsTer8
ENST00000478531.5:c.784+82del	ENSP00000420412.1:n.784+82del
ENST00000484087.5:c.409+82del	ENSP00000419481.1:n.409+82del
ENST00000487825.5:c.412+82del	ENSP00000418212.1:n.412+82del
ENST00000491747.6:c.787+82del	ENSP00000420705.2:n.787+82del
ENST00000492859.5:c.*805del	ENSP00000420253.1:n.*805del
ENST00000493795.5:c.728del	ENSP00000418775.1:p.Leu243TyrfsTer8
ENST00000493919.5:c.646+82del	ENSP00000418819.1:n.646+82del
ENST00000494123.5:c.869del	ENSP00000419103.1:p.Leu290TyrfsTer8
ENST00000497488.1:c.-20del	ENSP00000418986.1:n.-20del
ENST00000586385.5:c.4+30520del	ENSP00000465818.1:n.4+30520del
ENST00000591534.5:c.-43-20141del	ENSP00000467329.1:n.-43-20141del
ENST00000591849.5:c.-99+30609del	ENSP00000465347.1:n.-99+30609del
ENST00000634433.1:c.746del	ENSP00000489431.1:p.Leu249TyrfsTer8
NM_007294.3:c.869del , LRG_292t1:c.869del	NP_009225.1:p.Leu290TyrfsTer8
NM_007297.3:c.728del	NP_009228.2:p.Leu243TyrfsTer8
NM_007298.3:c.787+82del	NP_009229.2:n.787+82del
NM_007299.3:c.787+82del	NP_009230.2:n.787+82del
NM_007300.3:c.869del	NP_009231.2:p.Leu290TyrfsTer8
NR_027676.1:n.1005del
NM_007294.4:c.869del MANE Select	NP_009225.1:p.Leu290TyrfsTer8
NM_007297.4:c.728del	NP_009228.2:p.Leu243TyrfsTer8
NM_007299.4:c.787+82del	NP_009230.2:n.787+82del
NM_007300.4:c.869del	NP_009231.2:p.Leu290TyrfsTer8
NR_027676.2:n.1046del