Canonical Allele Identifier: CA2580612619

Gene: BRCA1

Linked Data

• ClinVar Variation Id: 1790927
• ClinVar RCV Id: RCV002450358

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093118_43093119del , CM000679.2:g.43093118_43093119del	GRCh38
NC_000017.10:g.41245135_41245136del , CM000679.1:g.41245135_41245136del	GRCh37
NC_000017.9:g.38498661_38498662del	NCBI36
NG_005905.2:g.124868_124869del , LRG_292:g.124868_124869del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2479_2480del
ENST00000461574.2:c.2415_2416del	ENSP00000417241.2:p.Ala806SerfsTer3
ENST00000470026.6:c.2415_2416del	ENSP00000419274.2:p.Ala806SerfsTer3
ENST00000473961.6:c.2289_2290del	ENSP00000420201.2:p.Ala764SerfsTer3
ENST00000476777.6:c.2412_2413del	ENSP00000417554.2:p.Ala805SerfsTer3
ENST00000477152.6:c.2337_2338del	ENSP00000419988.2:p.Ala780SerfsTer3
ENST00000478531.6:c.784+1628_784+1629del	ENSP00000420412.2:n.784+1628_784+1629del
ENST00000489037.2:c.2337_2338del	ENSP00000420781.2:p.Ala780SerfsTer3
ENST00000493919.6:c.646+1628_646+1629del	ENSP00000418819.2:n.646+1628_646+1629del
ENST00000494123.6:c.2415_2416del	ENSP00000419103.2:p.Ala806SerfsTer3
ENST00000497488.2:c.1527_1528del	ENSP00000418986.2:p.Ala510SerfsTer3
ENST00000618469.2:c.2415_2416del	ENSP00000478114.2:p.Ala806SerfsTer3
ENST00000634433.2:c.2292_2293del	ENSP00000489431.2:p.Ala765SerfsTer3
ENST00000644379.2:c.2415_2416del	ENSP00000496570.2:p.Ala806SerfsTer3
ENST00000644555.2:c.646+1628_646+1629del	ENSP00000494614.2:n.646+1628_646+1629del
ENST00000652672.2:c.2274_2275del	ENSP00000498906.2:p.Ala759SerfsTer3
ENST00000484087.6:c.664+1628_664+1629del	ENSP00000419481.2:n.664+1628_664+1629del
ENST00000700182.1:c.706+1628_706+1629del	ENSP00000514849.1:n.706+1628_706+1629del
ENST00000357654.9:c.2415_2416del MANE Select	ENSP00000350283.3:p.Ala806SerfsTer3
ENST00000471181.7:c.2415_2416del	ENSP00000418960.2:p.Ala806SerfsTer3
ENST00000352993.7:c.671-2084_671-2083del	ENSP00000312236.5:n.671-2084_671-2083del
ENST00000354071.7:c.2415_2416del	ENSP00000326002.7:p.Ala806SerfsTer3
ENST00000357654.7:c.2415_2416del	ENSP00000350283.3:p.Ala806SerfsTer3
ENST00000461221.5:c.*2198_*2199del	ENSP00000418548.1:n.*2198_*2199del
ENST00000468300.5:c.787+1628_787+1629del	ENSP00000417148.1:n.787+1628_787+1629del
ENST00000471181.6:c.2415_2416del	ENSP00000418960.2:p.Ala806SerfsTer3
ENST00000478531.5:c.784+1628_784+1629del	ENSP00000420412.1:n.784+1628_784+1629del
ENST00000484087.5:c.409+1628_409+1629del	ENSP00000419481.1:n.409+1628_409+1629del
ENST00000487825.5:c.412+1628_412+1629del	ENSP00000418212.1:n.412+1628_412+1629del
ENST00000491747.6:c.787+1628_787+1629del	ENSP00000420705.2:n.787+1628_787+1629del
ENST00000493795.5:c.2274_2275del	ENSP00000418775.1:p.Ala759SerfsTer3
ENST00000493919.5:c.646+1628_646+1629del	ENSP00000418819.1:n.646+1628_646+1629del
ENST00000586385.5:c.5-29165_5-29164del	ENSP00000465818.1:n.5-29165_5-29164del
ENST00000591534.5:c.-43-18595_-43-18594del	ENSP00000467329.1:n.-43-18595_-43-18594del
ENST00000591849.5:c.-99+32155_-99+32156del	ENSP00000465347.1:n.-99+32155_-99+32156del
ENST00000634433.1:c.2292_2293del	ENSP00000489431.1:p.Ala765SerfsTer3
NM_007294.3:c.2415_2416del , LRG_292t1:c.2415_2416del	NP_009225.1:p.Ala806SerfsTer3
NM_007297.3:c.2274_2275del	NP_009228.2:p.Ala759SerfsTer3
NM_007298.3:c.787+1628_787+1629del	NP_009229.2:n.787+1628_787+1629del
NM_007299.3:c.787+1628_787+1629del	NP_009230.2:n.787+1628_787+1629del
NM_007300.3:c.2415_2416del	NP_009231.2:p.Ala806SerfsTer3
NR_027676.1:n.2551_2552del
NM_007294.4:c.2415_2416del MANE Select	NP_009225.1:p.Ala806SerfsTer3
NM_007297.4:c.2274_2275del	NP_009228.2:p.Ala759SerfsTer3
NM_007299.4:c.787+1628_787+1629del	NP_009230.2:n.787+1628_787+1629del
NM_007300.4:c.2415_2416del	NP_009231.2:p.Ala806SerfsTer3
NR_027676.2:n.2592_2593del