Canonical Allele Identifier: CA1294885374
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399687T= , CM000664.2:g.144399687T= GRCh38
NC_000002.11:g.145157254T= , CM000664.1:g.145157254T= GRCh37
NC_000002.10:g.144873724T= NCBI36
NG_016431.1:g.125705A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1349A= ENSP00000508434.1:n.*1349A=
ENST00000440875.6:c.723A= ENSP00000475553.3:p.Glu241=
ENST00000627532.3:c.1500A= MANE Select ENSP00000487174.1:p.Glu500=
ENST00000636026.2:c.1500A= ENSP00000490776.1:p.Glu500=
ENST00000636179.1:n.1469A=
ENST00000636413.1:c.1164A= ENSP00000490508.1:p.Glu388=
ENST00000636471.1:c.1575A= ENSP00000490317.1:p.Glu525=
ENST00000636732.2:c.*1217A= ENSP00000490175.1:n.*1217A=
ENST00000636820.1:n.1600A=
ENST00000637045.1:c.1164A= ENSP00000490141.1:p.Glu388=
ENST00000637267.2:c.1500A= ENSP00000490293.2:p.Glu500=
ENST00000637304.1:c.1164A= ENSP00000490872.1:p.Glu388=
ENST00000638007.1:c.1164A= ENSP00000490723.1:p.Glu388=
ENST00000638087.1:c.1164A= ENSP00000490673.1:p.Glu388=
ENST00000638128.1:c.723A= ENSP00000490934.1:p.Glu241=
ENST00000675069.1:c.-133-837A= ENSP00000502467.1:n.-133-837A=
ENST00000675145.1:n.2048A=
ENST00000303660.8:c.1497A= ENSP00000302501.4:p.Glu499=
ENST00000409487.7:c.1500A= ENSP00000386854.2:p.Glu500=
ENST00000419938.5:c.655+1512A= ENSP00000394777.2:n.655+1512A=
ENST00000427902.5:c.1587A= ENSP00000395496.2:p.Glu529=
ENST00000440875.5:c.1154-137A= ENSP00000475553.2:n.1154-137A=
ENST00000539609.7:c.1428A= ENSP00000443792.2:p.Glu476=
ENST00000558170.6:c.1500A= ENSP00000454157.1:p.Glu500=
ENST00000627532.2:c.1500A= ENSP00000487174.1:p.Glu500=
NM_001171653.1:c.1428A= NP_001165124.1:p.Glu476=
NM_014795.3:c.1500A= NP_055610.1:p.Glu500=
XM_006712881.2:c.1500A= XP_006712944.1:p.Glu500=
XM_006712882.2:c.1500A= XP_006712945.1:p.Glu500=
XM_011512231.1:c.1491A= XP_011510533.1:p.Glu497=
XM_011512232.1:c.1479A= XP_011510534.1:p.Glu493=
NM_014795.4:c.1500A= MANE Select NP_055610.1:p.Glu500=
NM_001171653.2:c.1428A= NP_001165124.1:p.Glu476=