Canonical Allele Identifier: CA2260784283

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093745_43093746delinsGT , CM000679.2:g.43093745_43093746delinsGT	GRCh38
NC_000017.10:g.41245762_41245763delinsGT , CM000679.1:g.41245762_41245763delinsGT	GRCh37
NC_000017.9:g.38499288_38499289delinsGT	NCBI36
NG_005905.2:g.124238_124239delinsAC , LRG_292:g.124238_124239delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000354071.8:n.1849_1850delinsAC
ENST00000461574.2:c.1785_1786delinsAC	ENSP00000417241.2:p.Glu595=
ENST00000470026.6:c.1785_1786delinsAC	ENSP00000419274.2:p.Glu595=
ENST00000473961.6:c.1659_1660delinsAC	ENSP00000420201.2:p.Glu553=
ENST00000476777.6:c.1782_1783delinsAC	ENSP00000417554.2:p.Glu594=
ENST00000477152.6:c.1707_1708delinsAC	ENSP00000419988.2:p.Glu569=
ENST00000478531.6:c.784+998_784+999delinsAC	ENSP00000420412.2:n.784+998_784+999delinsAC
ENST00000489037.2:c.1707_1708delinsAC	ENSP00000420781.2:p.Glu569=
ENST00000493919.6:c.646+998_646+999delinsAC	ENSP00000418819.2:n.646+998_646+999delinsAC
ENST00000494123.6:c.1785_1786delinsAC	ENSP00000419103.2:p.Glu595=
ENST00000497488.2:c.897_898delinsAC	ENSP00000418986.2:p.Glu299=
ENST00000618469.2:c.1785_1786delinsAC	ENSP00000478114.2:p.Glu595=
ENST00000634433.2:c.1662_1663delinsAC	ENSP00000489431.2:p.Glu554=
ENST00000644379.2:c.1785_1786delinsAC	ENSP00000496570.2:p.Glu595=
ENST00000644555.2:c.646+998_646+999delinsAC	ENSP00000494614.2:n.646+998_646+999delinsAC
ENST00000652672.2:c.1644_1645delinsAC	ENSP00000498906.2:p.Glu548=
ENST00000484087.6:c.664+998_664+999delinsAC	ENSP00000419481.2:n.664+998_664+999delinsAC
ENST00000700182.1:c.706+998_706+999delinsAC	ENSP00000514849.1:n.706+998_706+999delinsAC
ENST00000357654.9:c.1785_1786delinsAC MANE Select	ENSP00000350283.3:p.Glu595=
ENST00000471181.7:c.1785_1786delinsAC	ENSP00000418960.2:p.Glu595=
ENST00000652672.1:c.1644_1645delinsAC	ENSP00000498906.1:p.Glu548=
ENST00000352993.7:c.670+2100_670+2101delinsAC	ENSP00000312236.5:n.670+2100_670+2101delinsAC
ENST00000354071.7:c.1785_1786delinsAC	ENSP00000326002.7:p.Glu595=
ENST00000357654.7:c.1785_1786delinsAC	ENSP00000350283.3:p.Glu595=
ENST00000412061.3:c.1136_1137delinsAC
ENST00000461221.5:c.*1568_*1569delinsAC	ENSP00000418548.1:n.*1568_*1569delinsAC
ENST00000468300.5:c.787+998_787+999delinsAC	ENSP00000417148.1:n.787+998_787+999delinsAC
ENST00000470026.5:c.1785_1786delinsAC	ENSP00000419274.1:p.Glu595=
ENST00000471181.6:c.1785_1786delinsAC	ENSP00000418960.2:p.Glu595=
ENST00000477152.5:c.1707_1708delinsAC	ENSP00000419988.1:p.Glu569=
ENST00000478531.5:c.784+998_784+999delinsAC	ENSP00000420412.1:n.784+998_784+999delinsAC
ENST00000484087.5:c.409+998_409+999delinsAC	ENSP00000419481.1:n.409+998_409+999delinsAC
ENST00000487825.5:c.412+998_412+999delinsAC	ENSP00000418212.1:n.412+998_412+999delinsAC
ENST00000491747.6:c.787+998_787+999delinsAC	ENSP00000420705.2:n.787+998_787+999delinsAC
ENST00000493795.5:c.1644_1645delinsAC	ENSP00000418775.1:p.Glu548=
ENST00000493919.5:c.646+998_646+999delinsAC	ENSP00000418819.1:n.646+998_646+999delinsAC
ENST00000586385.5:c.5-29795_5-29794delinsAC	ENSP00000465818.1:n.5-29795_5-29794delinsAC
ENST00000591534.5:c.-43-19225_-43-19224delinsAC	ENSP00000467329.1:n.-43-19225_-43-19224delinsAC
ENST00000591849.5:c.-99+31525_-99+31526delinsAC	ENSP00000465347.1:n.-99+31525_-99+31526delinsAC
ENST00000634433.1:c.1662_1663delinsAC	ENSP00000489431.1:p.Glu554=
NM_007294.3:c.1785_1786delinsAC , LRG_292t1:c.1785_1786delinsAC	NP_009225.1:p.Glu595=
NM_007297.3:c.1644_1645delinsAC	NP_009228.2:p.Glu548=
NM_007298.3:c.787+998_787+999delinsAC	NP_009229.2:n.787+998_787+999delinsAC
NM_007299.3:c.787+998_787+999delinsAC	NP_009230.2:n.787+998_787+999delinsAC
NM_007300.3:c.1785_1786delinsAC	NP_009231.2:p.Glu595=
NR_027676.1:n.1921_1922delinsAC
NM_007294.4:c.1785_1786delinsAC MANE Select	NP_009225.1:p.Glu595=
NM_007297.4:c.1644_1645delinsAC	NP_009228.2:p.Glu548=
NM_007299.4:c.787+998_787+999delinsAC	NP_009230.2:n.787+998_787+999delinsAC
NM_007300.4:c.1785_1786delinsAC	NP_009231.2:p.Glu595=
NR_027676.2:n.1962_1963delinsAC