Canonical Allele Identifier: CA2260783853
Gene: BRCA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.43093335_43093343delinsTTCTTTTTC , CM000679.2:g.43093335_43093343delinsTTCTTTTTC GRCh38
NC_000017.10:g.41245352_41245360delinsTTCTTTTTC , CM000679.1:g.41245352_41245360delinsTTCTTTTTC GRCh37
NC_000017.9:g.38498878_38498886delinsTTCTTTTTC NCBI36
NG_005905.2:g.124641_124649delinsGAAAAAGAA , LRG_292:g.124641_124649delinsGAAAAAGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000354071.8:n.2252_2260delinsGAAAAAGAA
ENST00000461574.2:c.2188_2196delinsGAAAAAGAA ENSP00000417241.2:p.Glu730=
ENST00000470026.6:c.2188_2196delinsGAAAAAGAA ENSP00000419274.2:p.Glu730=
ENST00000473961.6:c.2062_2070delinsGAAAAAGAA ENSP00000420201.2:p.Glu688=
ENST00000476777.6:c.2185_2193delinsGAAAAAGAA ENSP00000417554.2:p.Glu729=
ENST00000477152.6:c.2110_2118delinsGAAAAAGAA ENSP00000419988.2:p.Glu704=
ENST00000478531.6:c.784+1401_784+1409delinsGAAAAAGAA ENSP00000420412.2:n.784+1401_784+1409delinsGAAAAAGAA
ENST00000489037.2:c.2110_2118delinsGAAAAAGAA ENSP00000420781.2:p.Glu704=
ENST00000493919.6:c.646+1401_646+1409delinsGAAAAAGAA ENSP00000418819.2:n.646+1401_646+1409delinsGAAAAAGAA
ENST00000494123.6:c.2188_2196delinsGAAAAAGAA ENSP00000419103.2:p.Glu730=
ENST00000497488.2:c.1300_1308delinsGAAAAAGAA ENSP00000418986.2:p.Glu434=
ENST00000618469.2:c.2188_2196delinsGAAAAAGAA ENSP00000478114.2:p.Glu730=
ENST00000634433.2:c.2065_2073delinsGAAAAAGAA ENSP00000489431.2:p.Glu689=
ENST00000644379.2:c.2188_2196delinsGAAAAAGAA ENSP00000496570.2:p.Glu730=
ENST00000644555.2:c.646+1401_646+1409delinsGAAAAAGAA ENSP00000494614.2:n.646+1401_646+1409delinsGAAAAAGAA
ENST00000652672.2:c.2047_2055delinsGAAAAAGAA ENSP00000498906.2:p.Glu683=
ENST00000484087.6:c.664+1401_664+1409delinsGAAAAAGAA ENSP00000419481.2:n.664+1401_664+1409delinsGAAAAAGAA
ENST00000700182.1:c.706+1401_706+1409delinsGAAAAAGAA ENSP00000514849.1:n.706+1401_706+1409delinsGAAAAAGAA
ENST00000357654.9:c.2188_2196delinsGAAAAAGAA MANE Select ENSP00000350283.3:p.Glu730=
ENST00000471181.7:c.2188_2196delinsGAAAAAGAA ENSP00000418960.2:p.Glu730=
ENST00000352993.7:c.671-2311_671-2303delinsGAAAAAGAA ENSP00000312236.5:n.671-2311_671-2303delinsGAAAAAGAA
ENST00000354071.7:c.2188_2196delinsGAAAAAGAA ENSP00000326002.7:p.Glu730=
ENST00000357654.7:c.2188_2196delinsGAAAAAGAA ENSP00000350283.3:p.Glu730=
ENST00000461221.5:c.*1971_*1979delinsGAAAAAGAA ENSP00000418548.1:n.*1971_*1979delinsGAAAAAGAA
ENST00000468300.5:c.787+1401_787+1409delinsGAAAAAGAA ENSP00000417148.1:n.787+1401_787+1409delinsGAAAAAGAA
ENST00000471181.6:c.2188_2196delinsGAAAAAGAA ENSP00000418960.2:p.Glu730=
ENST00000478531.5:c.784+1401_784+1409delinsGAAAAAGAA ENSP00000420412.1:n.784+1401_784+1409delinsGAAAAAGAA
ENST00000484087.5:c.409+1401_409+1409delinsGAAAAAGAA ENSP00000419481.1:n.409+1401_409+1409delinsGAAAAAGAA
ENST00000487825.5:c.412+1401_412+1409delinsGAAAAAGAA ENSP00000418212.1:n.412+1401_412+1409delinsGAAAAAGAA
ENST00000491747.6:c.787+1401_787+1409delinsGAAAAAGAA ENSP00000420705.2:n.787+1401_787+1409delinsGAAAAAGAA
ENST00000493795.5:c.2047_2055delinsGAAAAAGAA ENSP00000418775.1:p.Glu683=
ENST00000493919.5:c.646+1401_646+1409delinsGAAAAAGAA ENSP00000418819.1:n.646+1401_646+1409delinsGAAAAAGAA
ENST00000586385.5:c.5-29392_5-29384delinsGAAAAAGAA ENSP00000465818.1:n.5-29392_5-29384delinsGAAAAAGAA
ENST00000591534.5:c.-43-18822_-43-18814delinsGAAAAAGAA ENSP00000467329.1:n.-43-18822_-43-18814delinsGAAAAAGAA
ENST00000591849.5:c.-99+31928_-99+31936delinsGAAAAAGAA ENSP00000465347.1:n.-99+31928_-99+31936delinsGAAAAAGAA
ENST00000634433.1:c.2065_2073delinsGAAAAAGAA ENSP00000489431.1:p.Glu689=
NM_007294.3:c.2188_2196delinsGAAAAAGAA , LRG_292t1:c.2188_2196delinsGAAAAAGAA NP_009225.1:p.Glu730=
NM_007297.3:c.2047_2055delinsGAAAAAGAA NP_009228.2:p.Glu683=
NM_007298.3:c.787+1401_787+1409delinsGAAAAAGAA NP_009229.2:n.787+1401_787+1409delinsGAAAAAGAA
NM_007299.3:c.787+1401_787+1409delinsGAAAAAGAA NP_009230.2:n.787+1401_787+1409delinsGAAAAAGAA
NM_007300.3:c.2188_2196delinsGAAAAAGAA NP_009231.2:p.Glu730=
NR_027676.1:n.2324_2332delinsGAAAAAGAA
NM_007294.4:c.2188_2196delinsGAAAAAGAA MANE Select NP_009225.1:p.Glu730=
NM_007297.4:c.2047_2055delinsGAAAAAGAA NP_009228.2:p.Glu683=
NM_007299.4:c.787+1401_787+1409delinsGAAAAAGAA NP_009230.2:n.787+1401_787+1409delinsGAAAAAGAA
NM_007300.4:c.2188_2196delinsGAAAAAGAA NP_009231.2:p.Glu730=
NR_027676.2:n.2365_2373delinsGAAAAAGAA