Canonical Allele Identifier: CA253277
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144400012_144400015del , CM000664.2:g.144400012_144400015del GRCh38
NC_000002.11:g.145157579_145157582del , CM000664.1:g.145157579_145157582del GRCh37
NC_000002.10:g.144874049_144874052del NCBI36
NG_016431.1:g.125378_125381del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1022_*1025del ENSP00000508434.1:n.*1022_*1025del
ENST00000440875.6:c.396_399del ENSP00000475553.3:p.Thr133AsnfsTer3
ENST00000627532.3:c.1173_1176del MANE Select ENSP00000487174.1:p.Thr392AsnfsTer3
ENST00000636026.2:c.1173_1176del ENSP00000490776.1:p.Thr392AsnfsTer3
ENST00000636179.1:n.1142_1145del
ENST00000636413.1:c.837_840del ENSP00000490508.1:p.Thr280AsnfsTer3
ENST00000636471.1:c.1248_1251del ENSP00000490317.1:p.Thr417AsnfsTer3
ENST00000636732.2:c.*890_*893del ENSP00000490175.1:n.*890_*893del
ENST00000636820.1:n.1273_1276del
ENST00000637045.1:c.837_840del ENSP00000490141.1:p.Thr280AsnfsTer3
ENST00000637267.2:c.1173_1176del ENSP00000490293.2:p.Thr392AsnfsTer3
ENST00000637304.1:c.837_840del ENSP00000490872.1:p.Thr280AsnfsTer3
ENST00000638007.1:c.837_840del ENSP00000490723.1:p.Thr280AsnfsTer3
ENST00000638087.1:c.837_840del ENSP00000490673.1:p.Thr280AsnfsTer3
ENST00000638128.1:c.396_399del ENSP00000490934.1:p.Thr133AsnfsTer3
ENST00000675069.1:c.-133-1164_-133-1161del ENSP00000502467.1:n.-133-1164_-133-1161del
ENST00000675145.1:n.1721_1724del
ENST00000303660.8:c.1170_1173del ENSP00000302501.4:p.Thr391AsnfsTer3
ENST00000392861.6:c.1257_1260del ENSP00000376601.3:p.Thr420AsnfsTer3
ENST00000409487.7:c.1173_1176del ENSP00000386854.2:p.Thr392AsnfsTer3
ENST00000419938.5:c.655+1185_655+1188del ENSP00000394777.2:n.655+1185_655+1188del
ENST00000427902.5:c.1260_1263del ENSP00000395496.2:p.Thr421AsnfsTer3
ENST00000440875.5:c.1153+5_1153+8del ENSP00000475553.2:n.1153+5_1153+8del
ENST00000539609.7:c.1101_1104del ENSP00000443792.2:p.Thr368AsnfsTer3
ENST00000558170.6:c.1173_1176del ENSP00000454157.1:p.Thr392AsnfsTer3
ENST00000627532.2:c.1173_1176del ENSP00000487174.1:p.Thr392AsnfsTer3
NM_001171653.1:c.1101_1104del NP_001165124.1:p.Thr368AsnfsTer3
NM_014795.3:c.1173_1176del NP_055610.1:p.Thr392AsnfsTer3
XM_006712881.2:c.1173_1176del XP_006712944.1:p.Thr392AsnfsTer3
XM_006712882.2:c.1173_1176del XP_006712945.1:p.Thr392AsnfsTer3
XM_011512231.1:c.1164_1167del XP_011510533.1:p.Thr389AsnfsTer3
XM_011512232.1:c.1152_1155del XP_011510534.1:p.Thr385AsnfsTer3
NM_014795.4:c.1173_1176del MANE Select NP_055610.1:p.Thr392AsnfsTer3
NM_001171653.2:c.1101_1104del NP_001165124.1:p.Thr368AsnfsTer3