Canonical Allele Identifier: CA2260783708

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093207_43093220delinsGTACCAGGTACCAA , CM000679.2:g.43093207_43093220delinsGTACCAGGTACCAA	GRCh38
NC_000017.10:g.41245224_41245237delinsGTACCAGGTACCAA , CM000679.1:g.41245224_41245237delinsGTACCAGGTACCAA	GRCh37
NC_000017.9:g.38498750_38498763delinsGTACCAGGTACCAA	NCBI36
NG_005905.2:g.124764_124777delinsTTGGTACCTGGTAC , LRG_292:g.124764_124777delinsTTGGTACCTGGTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.2375_2388delinsTTGGTACCTGGTAC
ENST00000461574.2:c.2311_2324delinsTTGGTACCTGGTAC	ENSP00000417241.2:p.Leu771=
ENST00000470026.6:c.2311_2324delinsTTGGTACCTGGTAC	ENSP00000419274.2:p.Leu771=
ENST00000473961.6:c.2185_2198delinsTTGGTACCTGGTAC	ENSP00000420201.2:p.Leu729=
ENST00000476777.6:c.2308_2321delinsTTGGTACCTGGTAC	ENSP00000417554.2:p.Leu770=
ENST00000477152.6:c.2233_2246delinsTTGGTACCTGGTAC	ENSP00000419988.2:p.Leu745=
ENST00000478531.6:c.784+1524_784+1537delinsTTGGTACCTGGTAC	ENSP00000420412.2:n.784+1524_784+1537delinsTTGGTACCTGGTAC
ENST00000489037.2:c.2233_2246delinsTTGGTACCTGGTAC	ENSP00000420781.2:p.Leu745=
ENST00000493919.6:c.646+1524_646+1537delinsTTGGTACCTGGTAC	ENSP00000418819.2:n.646+1524_646+1537delinsTTGGTACCTGGTAC
ENST00000494123.6:c.2311_2324delinsTTGGTACCTGGTAC	ENSP00000419103.2:p.Leu771=
ENST00000497488.2:c.1423_1436delinsTTGGTACCTGGTAC	ENSP00000418986.2:p.Leu475=
ENST00000618469.2:c.2311_2324delinsTTGGTACCTGGTAC	ENSP00000478114.2:p.Leu771=
ENST00000634433.2:c.2188_2201delinsTTGGTACCTGGTAC	ENSP00000489431.2:p.Leu730=
ENST00000644379.2:c.2311_2324delinsTTGGTACCTGGTAC	ENSP00000496570.2:p.Leu771=
ENST00000644555.2:c.646+1524_646+1537delinsTTGGTACCTGGTAC	ENSP00000494614.2:n.646+1524_646+1537delinsTTGGTACCTGGTAC
ENST00000652672.2:c.2170_2183delinsTTGGTACCTGGTAC	ENSP00000498906.2:p.Leu724=
ENST00000484087.6:c.664+1524_664+1537delinsTTGGTACCTGGTAC	ENSP00000419481.2:n.664+1524_664+1537delinsTTGGTACCTGGTAC
ENST00000700182.1:c.706+1524_706+1537delinsTTGGTACCTGGTAC	ENSP00000514849.1:n.706+1524_706+1537delinsTTGGTACCTGGTAC
ENST00000357654.9:c.2311_2324delinsTTGGTACCTGGTAC MANE Select	ENSP00000350283.3:p.Leu771=
ENST00000471181.7:c.2311_2324delinsTTGGTACCTGGTAC	ENSP00000418960.2:p.Leu771=
ENST00000352993.7:c.671-2188_671-2175delinsTTGGTACCTGGTAC	ENSP00000312236.5:n.671-2188_671-2175delinsTTGGTACCTGGTAC
ENST00000354071.7:c.2311_2324delinsTTGGTACCTGGTAC	ENSP00000326002.7:p.Leu771=
ENST00000357654.7:c.2311_2324delinsTTGGTACCTGGTAC	ENSP00000350283.3:p.Leu771=
ENST00000461221.5:c.*2094_*2107delinsTTGGTACCTGGTAC	ENSP00000418548.1:n.*2094_*2107delinsTTGGTACCTGGTAC
ENST00000468300.5:c.787+1524_787+1537delinsTTGGTACCTGGTAC	ENSP00000417148.1:n.787+1524_787+1537delinsTTGGTACCTGGTAC
ENST00000471181.6:c.2311_2324delinsTTGGTACCTGGTAC	ENSP00000418960.2:p.Leu771=
ENST00000478531.5:c.784+1524_784+1537delinsTTGGTACCTGGTAC	ENSP00000420412.1:n.784+1524_784+1537delinsTTGGTACCTGGTAC
ENST00000484087.5:c.409+1524_409+1537delinsTTGGTACCTGGTAC	ENSP00000419481.1:n.409+1524_409+1537delinsTTGGTACCTGGTAC
ENST00000487825.5:c.412+1524_412+1537delinsTTGGTACCTGGTAC	ENSP00000418212.1:n.412+1524_412+1537delinsTTGGTACCTGGTAC
ENST00000491747.6:c.787+1524_787+1537delinsTTGGTACCTGGTAC	ENSP00000420705.2:n.787+1524_787+1537delinsTTGGTACCTGGTAC
ENST00000493795.5:c.2170_2183delinsTTGGTACCTGGTAC	ENSP00000418775.1:p.Leu724=
ENST00000493919.5:c.646+1524_646+1537delinsTTGGTACCTGGTAC	ENSP00000418819.1:n.646+1524_646+1537delinsTTGGTACCTGGTAC
ENST00000586385.5:c.5-29269_5-29256delinsTTGGTACCTGGTAC	ENSP00000465818.1:n.5-29269_5-29256delinsTTGGTACCTGGTAC
ENST00000591534.5:c.-43-18699_-43-18686delinsTTGGTACCTGGTAC	ENSP00000467329.1:n.-43-18699_-43-18686delinsTTGGTACCTGGTAC
ENST00000591849.5:c.-99+32051_-99+32064delinsTTGGTACCTGGTAC	ENSP00000465347.1:n.-99+32051_-99+32064delinsTTGGTACCTGGTAC
ENST00000634433.1:c.2188_2201delinsTTGGTACCTGGTAC	ENSP00000489431.1:p.Leu730=
NM_007294.3:c.2311_2324delinsTTGGTACCTGGTAC , LRG_292t1:c.2311_2324delinsTTGGTACCTGGTAC	NP_009225.1:p.Leu771=
NM_007297.3:c.2170_2183delinsTTGGTACCTGGTAC	NP_009228.2:p.Leu724=
NM_007298.3:c.787+1524_787+1537delinsTTGGTACCTGGTAC	NP_009229.2:n.787+1524_787+1537delinsTTGGTACCTGGTAC
NM_007299.3:c.787+1524_787+1537delinsTTGGTACCTGGTAC	NP_009230.2:n.787+1524_787+1537delinsTTGGTACCTGGTAC
NM_007300.3:c.2311_2324delinsTTGGTACCTGGTAC	NP_009231.2:p.Leu771=
NR_027676.1:n.2447_2460delinsTTGGTACCTGGTAC
NM_007294.4:c.2311_2324delinsTTGGTACCTGGTAC MANE Select	NP_009225.1:p.Leu771=
NM_007297.4:c.2170_2183delinsTTGGTACCTGGTAC	NP_009228.2:p.Leu724=
NM_007299.4:c.787+1524_787+1537delinsTTGGTACCTGGTAC	NP_009230.2:n.787+1524_787+1537delinsTTGGTACCTGGTAC
NM_007300.4:c.2311_2324delinsTTGGTACCTGGTAC	NP_009231.2:p.Leu771=
NR_027676.2:n.2488_2501delinsTTGGTACCTGGTAC