Canonical Allele Identifier: CA295846
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144429811del , CM000664.2:g.144429811del GRCh38
NC_000002.11:g.145187378del , CM000664.1:g.145187378del GRCh37
NC_000002.10:g.144903848del NCBI36
NG_016431.1:g.95581del

Transcript Alleles

HGVS Amino-acid Change
ENST00000637591.2:n.438del
ENST00000689298.1:c.*210del ENSP00000508434.1:n.*210del
ENST00000440875.6:c.-417del ENSP00000475553.3:n.-417del
ENST00000627532.3:c.289del MANE Select ENSP00000487174.1:p.Trp97GlyfsTer11
ENST00000636026.2:c.289del ENSP00000490776.1:p.Trp97GlyfsTer11
ENST00000636179.1:n.258del
ENST00000636413.1:c.-48del ENSP00000490508.1:n.-48del
ENST00000636471.1:c.289del ENSP00000490317.1:p.Trp97GlyfsTer11
ENST00000636732.2:c.289del ENSP00000490175.1:p.Trp97GlyfsTer11
ENST00000636820.1:n.389del
ENST00000637045.1:c.-48del ENSP00000490141.1:n.-48del
ENST00000637267.2:c.289del ENSP00000490293.2:p.Trp97GlyfsTer11
ENST00000637304.1:c.-48del ENSP00000490872.1:n.-48del
ENST00000638007.1:c.-48del ENSP00000490723.1:n.-48del
ENST00000638087.1:c.-48del ENSP00000490673.1:n.-48del
ENST00000638128.1:c.-417del ENSP00000490934.1:n.-417del
ENST00000675069.1:c.-133-30961del ENSP00000502467.1:n.-133-30961del
ENST00000303660.8:c.289del ENSP00000302501.4:p.Trp97GlyfsTer11
ENST00000392861.6:c.373del ENSP00000376601.3:p.Trp125GlyfsTer11
ENST00000409211.5:c.289del ENSP00000387256.2:p.Trp97GlyfsTer11
ENST00000409487.7:c.289del ENSP00000386854.2:p.Trp97GlyfsTer11
ENST00000419938.5:c.289del ENSP00000394777.2:p.Trp97GlyfsTer11
ENST00000427902.5:c.376del ENSP00000395496.2:p.Trp126GlyfsTer11
ENST00000431672.4:c.289del ENSP00000475267.2:p.Trp97GlyfsTer11
ENST00000434448.5:c.*220del ENSP00000487261.1:n.*220del
ENST00000440875.5:c.274del ENSP00000475553.2:p.Trp92GlyfsTer11
ENST00000461784.3:n.496del
ENST00000465308.5:c.289del ENSP00000487476.1:p.Trp97GlyfsTer11
ENST00000472146.5:n.539del
ENST00000476394.5:n.393del
ENST00000479735.1:n.520del
ENST00000539609.7:c.289del ENSP00000443792.2:p.Trp97GlyfsTer11
ENST00000558170.6:c.289del ENSP00000454157.1:p.Trp97GlyfsTer11
ENST00000627532.2:c.289del ENSP00000487174.1:p.Trp97GlyfsTer11
ENST00000627856.2:n.249del
NM_001171653.1:c.289del NP_001165124.1:p.Trp97GlyfsTer11
NM_014795.3:c.289del NP_055610.1:p.Trp97GlyfsTer11
XM_006712881.2:c.289del XP_006712944.1:p.Trp97GlyfsTer11
XM_006712882.2:c.289del XP_006712945.1:p.Trp97GlyfsTer11
XM_011512231.1:c.280del XP_011510533.1:p.Trp94GlyfsTer11
XM_011512232.1:c.268del XP_011510534.1:p.Trp90GlyfsTer11
NM_014795.4:c.289del MANE Select NP_055610.1:p.Trp97GlyfsTer11
NM_001171653.2:c.289del NP_001165124.1:p.Trp97GlyfsTer11