Canonical Allele Identifier: CA2586970117
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399521del , CM000664.2:g.144399521del GRCh38
NC_000002.11:g.145157088del , CM000664.1:g.145157088del GRCh37
NC_000002.10:g.144873558del NCBI36
NG_016431.1:g.125873del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1517del ENSP00000508434.1:n.*1517del
ENST00000440875.6:c.891del ENSP00000475553.3:p.Glu298ArgfsTer6
ENST00000627532.3:c.1668del MANE Select ENSP00000487174.1:p.Glu557ArgfsTer6
ENST00000636026.2:c.1668del ENSP00000490776.1:p.Glu557ArgfsTer6
ENST00000636179.1:n.1637del
ENST00000636413.1:c.1332del ENSP00000490508.1:p.Glu445ArgfsTer6
ENST00000636471.1:c.1743del ENSP00000490317.1:p.Glu582ArgfsTer6
ENST00000636732.2:c.*1385del ENSP00000490175.1:n.*1385del
ENST00000636820.1:n.1768del
ENST00000637045.1:c.1332del ENSP00000490141.1:p.Glu445ArgfsTer6
ENST00000637267.2:c.1668del ENSP00000490293.2:p.Glu557ArgfsTer6
ENST00000637304.1:c.1332del ENSP00000490872.1:p.Glu445ArgfsTer6
ENST00000638007.1:c.1332del ENSP00000490723.1:p.Glu445ArgfsTer6
ENST00000638087.1:c.1332del ENSP00000490673.1:p.Glu445ArgfsTer6
ENST00000638128.1:c.891del ENSP00000490934.1:p.Glu298ArgfsTer6
ENST00000675069.1:c.-133-669del ENSP00000502467.1:n.-133-669del
ENST00000675145.1:n.2216del
ENST00000303660.8:c.1665del ENSP00000302501.4:p.Glu556ArgfsTer6
ENST00000409487.7:c.1668del ENSP00000386854.2:p.Glu557ArgfsTer6
ENST00000419938.5:c.655+1680del ENSP00000394777.2:n.655+1680del
ENST00000427902.5:c.1755del ENSP00000395496.2:p.Glu586ArgfsTer6
ENST00000440875.5:c.1167+18del ENSP00000475553.2:n.1167+18del
ENST00000539609.7:c.1596del ENSP00000443792.2:p.Glu533ArgfsTer6
ENST00000558170.6:c.1668del ENSP00000454157.1:p.Glu557ArgfsTer6
ENST00000627532.2:c.1668del ENSP00000487174.1:p.Glu557ArgfsTer6
NM_001171653.1:c.1596del NP_001165124.1:p.Glu533ArgfsTer6
NM_014795.3:c.1668del NP_055610.1:p.Glu557ArgfsTer6
XM_006712881.2:c.1668del XP_006712944.1:p.Glu557ArgfsTer6
XM_006712882.2:c.1668del XP_006712945.1:p.Glu557ArgfsTer6
XM_011512231.1:c.1659del XP_011510533.1:p.Glu554ArgfsTer6
XM_011512232.1:c.1647del XP_011510534.1:p.Glu550ArgfsTer6
NM_014795.4:c.1668del MANE Select NP_055610.1:p.Glu557ArgfsTer6
NM_001171653.2:c.1596del NP_001165124.1:p.Glu533ArgfsTer6