Canonical Allele Identifier: CA1294885161
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399108T= , CM000664.2:g.144399108T= GRCh38
NC_000002.11:g.145156675T= , CM000664.1:g.145156675T= GRCh37
NC_000002.10:g.144873145T= NCBI36
NG_016431.1:g.126284A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1928A= ENSP00000508434.1:n.*1928A=
ENST00000440875.6:c.1302A= ENSP00000475553.3:p.Glu434=
ENST00000627532.3:c.2079A= MANE Select ENSP00000487174.1:p.Glu693=
ENST00000636026.2:c.2079A= ENSP00000490776.1:p.Glu693=
ENST00000636179.1:n.2048A=
ENST00000636413.1:c.1743A= ENSP00000490508.1:p.Glu581=
ENST00000636471.1:c.2154A= ENSP00000490317.1:p.Glu718=
ENST00000636732.2:c.*1796A= ENSP00000490175.1:n.*1796A=
ENST00000636820.1:n.2179A=
ENST00000637045.1:c.1743A= ENSP00000490141.1:p.Glu581=
ENST00000637304.1:c.1743A= ENSP00000490872.1:p.Glu581=
ENST00000638007.1:c.1743A= ENSP00000490723.1:p.Glu581=
ENST00000638087.1:c.1743A= ENSP00000490673.1:p.Glu581=
ENST00000638128.1:c.1302A= ENSP00000490934.1:p.Glu434=
ENST00000675069.1:c.-133-258A= ENSP00000502467.1:n.-133-258A=
ENST00000675145.1:n.2627A=
ENST00000303660.8:c.2076A= ENSP00000302501.4:p.Glu692=
ENST00000409487.7:c.2079A= ENSP00000386854.2:p.Glu693=
ENST00000419938.5:c.655+2091A= ENSP00000394777.2:n.655+2091A=
ENST00000427902.5:c.2166A= ENSP00000395496.2:p.Glu722=
ENST00000440875.5:c.1167+429A= ENSP00000475553.2:n.1167+429A=
ENST00000539609.7:c.2007A= ENSP00000443792.2:p.Glu669=
ENST00000558170.6:c.2079A= ENSP00000454157.1:p.Glu693=
ENST00000627532.2:c.2079A= ENSP00000487174.1:p.Glu693=
NM_001171653.1:c.2007A= NP_001165124.1:p.Glu669=
NM_014795.3:c.2079A= NP_055610.1:p.Glu693=
XM_006712881.2:c.2079A= XP_006712944.1:p.Glu693=
XM_006712882.2:c.2079A= XP_006712945.1:p.Glu693=
XM_011512231.1:c.2070A= XP_011510533.1:p.Glu690=
XM_011512232.1:c.2058A= XP_011510534.1:p.Glu686=
NM_014795.4:c.2079A= MANE Select NP_055610.1:p.Glu693=
NM_001171653.2:c.2007A= NP_001165124.1:p.Glu669=