Canonical Allele Identifier: CA2832528733
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399107del , CM000664.2:g.144399107del GRCh38
NC_000002.11:g.145156674del , CM000664.1:g.145156674del GRCh37
NC_000002.10:g.144873144del NCBI36
NG_016431.1:g.126285del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1929del ENSP00000508434.1:n.*1929del
ENST00000440875.6:c.1303del ENSP00000475553.3:p.Gln435AsnfsTer22
ENST00000627532.3:c.2080del MANE Select ENSP00000487174.1:p.Gln694AsnfsTer22
ENST00000636026.2:c.2080del ENSP00000490776.1:p.Gln694AsnfsTer22
ENST00000636179.1:n.2049del
ENST00000636413.1:c.1744del ENSP00000490508.1:p.Gln582AsnfsTer22
ENST00000636471.1:c.2155del ENSP00000490317.1:p.Gln719AsnfsTer22
ENST00000636732.2:c.*1797del ENSP00000490175.1:n.*1797del
ENST00000636820.1:n.2180del
ENST00000637045.1:c.1744del ENSP00000490141.1:p.Gln582AsnfsTer22
ENST00000637304.1:c.1744del ENSP00000490872.1:p.Gln582AsnfsTer22
ENST00000638007.1:c.1744del ENSP00000490723.1:p.Gln582AsnfsTer22
ENST00000638087.1:c.1744del ENSP00000490673.1:p.Gln582AsnfsTer22
ENST00000638128.1:c.1303del ENSP00000490934.1:p.Gln435AsnfsTer22
ENST00000675069.1:c.-133-257del ENSP00000502467.1:n.-133-257del
ENST00000675145.1:n.2628del
ENST00000303660.8:c.2077del ENSP00000302501.4:p.Gln693AsnfsTer22
ENST00000409487.7:c.2080del ENSP00000386854.2:p.Gln694AsnfsTer22
ENST00000419938.5:c.655+2092del ENSP00000394777.2:n.655+2092del
ENST00000427902.5:c.2167del ENSP00000395496.2:p.Gln723AsnfsTer?
ENST00000440875.5:c.1167+430del ENSP00000475553.2:n.1167+430del
ENST00000539609.7:c.2008del ENSP00000443792.2:p.Gln670AsnfsTer22
ENST00000558170.6:c.2080del ENSP00000454157.1:p.Gln694AsnfsTer22
ENST00000627532.2:c.2080del ENSP00000487174.1:p.Gln694AsnfsTer22
NM_001171653.1:c.2008del NP_001165124.1:p.Gln670AsnfsTer22
NM_014795.3:c.2080del NP_055610.1:p.Gln694AsnfsTer22
XM_006712881.2:c.2080del XP_006712944.1:p.Gln694AsnfsTer22
XM_006712882.2:c.2080del XP_006712945.1:p.Gln694AsnfsTer22
XM_011512231.1:c.2071del XP_011510533.1:p.Gln691AsnfsTer22
XM_011512232.1:c.2059del XP_011510534.1:p.Gln687AsnfsTer22
NM_014795.4:c.2080del MANE Select NP_055610.1:p.Gln694AsnfsTer22
NM_001171653.2:c.2008del NP_001165124.1:p.Gln670AsnfsTer22