Canonical Allele Identifier: CA2499224529

Gene: BRCA1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.43093608_43093609insT , CM000679.2:g.43093608_43093609insT	GRCh38
NC_000017.10:g.41245625_41245626insT , CM000679.1:g.41245625_41245626insT	GRCh37
NC_000017.9:g.38499151_38499152insT	NCBI36
NG_005905.2:g.124375_124376insA , LRG_292:g.124375_124376insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354071.8:n.1986_1987insA
ENST00000461574.2:c.1922_1923insA	ENSP00000417241.2:p.Asp642Ter
ENST00000470026.6:c.1922_1923insA	ENSP00000419274.2:p.Asp642Ter
ENST00000473961.6:c.1796_1797insA	ENSP00000420201.2:p.Asp600Ter
ENST00000476777.6:c.1919_1920insA	ENSP00000417554.2:p.Asp641Ter
ENST00000477152.6:c.1844_1845insA	ENSP00000419988.2:p.Asp616Ter
ENST00000478531.6:c.784+1135_784+1136insA	ENSP00000420412.2:n.784+1135_784+1136insA
ENST00000489037.2:c.1844_1845insA	ENSP00000420781.2:p.Asp616Ter
ENST00000493919.6:c.646+1135_646+1136insA	ENSP00000418819.2:n.646+1135_646+1136insA
ENST00000494123.6:c.1922_1923insA	ENSP00000419103.2:p.Asp642Ter
ENST00000497488.2:c.1034_1035insA	ENSP00000418986.2:p.Asp346Ter
ENST00000618469.2:c.1922_1923insA	ENSP00000478114.2:p.Asp642Ter
ENST00000634433.2:c.1799_1800insA	ENSP00000489431.2:p.Asp601Ter
ENST00000644379.2:c.1922_1923insA	ENSP00000496570.2:p.Asp642Ter
ENST00000644555.2:c.646+1135_646+1136insA	ENSP00000494614.2:n.646+1135_646+1136insA
ENST00000652672.2:c.1781_1782insA	ENSP00000498906.2:p.Asp595Ter
ENST00000484087.6:c.664+1135_664+1136insA	ENSP00000419481.2:n.664+1135_664+1136insA
ENST00000700182.1:c.706+1135_706+1136insA	ENSP00000514849.1:n.706+1135_706+1136insA
ENST00000357654.9:c.1922_1923insA MANE Select	ENSP00000350283.3:p.Asp642Ter
ENST00000471181.7:c.1922_1923insA	ENSP00000418960.2:p.Asp642Ter
ENST00000652672.1:c.1781_1782insA	ENSP00000498906.1:p.Asp595Ter
ENST00000352993.7:c.670+2237_670+2238insA	ENSP00000312236.5:n.670+2237_670+2238insA
ENST00000354071.7:c.1922_1923insA	ENSP00000326002.7:p.Asp642Ter
ENST00000357654.7:c.1922_1923insA	ENSP00000350283.3:p.Asp642Ter
ENST00000412061.3:c.1273_1274insA
ENST00000461221.5:c.*1705_*1706insA	ENSP00000418548.1:n.*1705_*1706insA
ENST00000468300.5:c.787+1135_787+1136insA	ENSP00000417148.1:n.787+1135_787+1136insA
ENST00000470026.5:c.1922_1923insA	ENSP00000419274.1:p.Asp642Ter
ENST00000471181.6:c.1922_1923insA	ENSP00000418960.2:p.Asp642Ter
ENST00000477152.5:c.1844_1845insA	ENSP00000419988.1:p.Asp616Ter
ENST00000478531.5:c.784+1135_784+1136insA	ENSP00000420412.1:n.784+1135_784+1136insA
ENST00000484087.5:c.409+1135_409+1136insA	ENSP00000419481.1:n.409+1135_409+1136insA
ENST00000487825.5:c.412+1135_412+1136insA	ENSP00000418212.1:n.412+1135_412+1136insA
ENST00000491747.6:c.787+1135_787+1136insA	ENSP00000420705.2:n.787+1135_787+1136insA
ENST00000493795.5:c.1781_1782insA	ENSP00000418775.1:p.Asp595Ter
ENST00000493919.5:c.646+1135_646+1136insA	ENSP00000418819.1:n.646+1135_646+1136insA
ENST00000586385.5:c.5-29658_5-29657insA	ENSP00000465818.1:n.5-29658_5-29657insA
ENST00000591534.5:c.-43-19088_-43-19087insA	ENSP00000467329.1:n.-43-19088_-43-19087insA
ENST00000591849.5:c.-99+31662_-99+31663insA	ENSP00000465347.1:n.-99+31662_-99+31663insA
ENST00000634433.1:c.1799_1800insA	ENSP00000489431.1:p.Asp601Ter
NM_007294.3:c.1922_1923insA , LRG_292t1:c.1922_1923insA	NP_009225.1:p.Asp642Ter
NM_007297.3:c.1781_1782insA	NP_009228.2:p.Asp595Ter
NM_007298.3:c.787+1135_787+1136insA	NP_009229.2:n.787+1135_787+1136insA
NM_007299.3:c.787+1135_787+1136insA	NP_009230.2:n.787+1135_787+1136insA
NM_007300.3:c.1922_1923insA	NP_009231.2:p.Asp642Ter
NR_027676.1:n.2058_2059insA
NM_007294.4:c.1922_1923insA MANE Select	NP_009225.1:p.Asp642Ter
NM_007297.4:c.1781_1782insA	NP_009228.2:p.Asp595Ter
NM_007299.4:c.787+1135_787+1136insA	NP_009230.2:n.787+1135_787+1136insA
NM_007300.4:c.1922_1923insA	NP_009231.2:p.Asp642Ter
NR_027676.2:n.2099_2100insA