Canonical Allele Identifier: CA2586965040
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144404072del , CM000664.2:g.144404072del GRCh38
NC_000002.11:g.145161639del , CM000664.1:g.145161639del GRCh37
NC_000002.10:g.144878109del NCBI36
NG_016431.1:g.121321del

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*501del ENSP00000508434.1:n.*501del
ENST00000440875.6:c.-126del ENSP00000475553.3:n.-126del
ENST00000627532.3:c.652del MANE Select ENSP00000487174.1:p.Arg218GlyfsTer6
ENST00000636026.2:c.652del ENSP00000490776.1:p.Arg218GlyfsTer6
ENST00000636179.1:n.621del
ENST00000636413.1:c.316del ENSP00000490508.1:p.Arg106GlyfsTer6
ENST00000636471.1:c.652del ENSP00000490317.1:p.Arg218GlyfsTer6
ENST00000636732.2:c.*369del ENSP00000490175.1:n.*369del
ENST00000636820.1:n.752del
ENST00000637045.1:c.316del ENSP00000490141.1:p.Arg106GlyfsTer6
ENST00000637267.2:c.652del ENSP00000490293.2:p.Arg218GlyfsTer6
ENST00000637304.1:c.316del ENSP00000490872.1:p.Arg106GlyfsTer6
ENST00000638007.1:c.316del ENSP00000490723.1:p.Arg106GlyfsTer6
ENST00000638087.1:c.316del ENSP00000490673.1:p.Arg106GlyfsTer6
ENST00000638128.1:c.-126del ENSP00000490934.1:n.-126del
ENST00000675069.1:c.-133-5221del ENSP00000502467.1:n.-133-5221del
ENST00000303660.8:c.649del ENSP00000302501.4:p.Arg217GlyfsTer6
ENST00000392861.6:c.736del ENSP00000376601.3:p.Arg246GlyfsTer6
ENST00000409487.7:c.652del ENSP00000386854.2:p.Arg218GlyfsTer6
ENST00000419938.5:c.391del ENSP00000394777.2:p.Arg131GlyfsTer6
ENST00000427902.5:c.739del ENSP00000395496.2:p.Arg247GlyfsTer6
ENST00000440875.5:c.637del ENSP00000475553.2:p.Arg213GlyfsTer6
ENST00000497268.1:n.598del
ENST00000539609.7:c.580del ENSP00000443792.2:p.Arg194GlyfsTer6
ENST00000558170.6:c.652del ENSP00000454157.1:p.Arg218GlyfsTer6
ENST00000627532.2:c.652del ENSP00000487174.1:p.Arg218GlyfsTer6
NM_001171653.1:c.580del NP_001165124.1:p.Arg194GlyfsTer6
NM_014795.3:c.652del NP_055610.1:p.Arg218GlyfsTer6
XM_006712881.2:c.652del XP_006712944.1:p.Arg218GlyfsTer6
XM_006712882.2:c.652del XP_006712945.1:p.Arg218GlyfsTer6
XM_011512231.1:c.643del XP_011510533.1:p.Arg215GlyfsTer6
XM_011512232.1:c.631del XP_011510534.1:p.Arg211GlyfsTer6
NM_014795.4:c.652del MANE Select NP_055610.1:p.Arg218GlyfsTer6
NM_001171653.2:c.580del NP_001165124.1:p.Arg194GlyfsTer6