Canonical Allele Identifier: CA1294885349
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399622G= , CM000664.2:g.144399622G= GRCh38
NC_000002.11:g.145157189G= , CM000664.1:g.145157189G= GRCh37
NC_000002.10:g.144873659G= NCBI36
NG_016431.1:g.125770C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1414C= ENSP00000508434.1:n.*1414C=
ENST00000440875.6:c.788C= ENSP00000475553.3:p.Thr263=
ENST00000627532.3:c.1565C= MANE Select ENSP00000487174.1:p.Thr522=
ENST00000636026.2:c.1565C= ENSP00000490776.1:p.Thr522=
ENST00000636179.1:n.1534C=
ENST00000636413.1:c.1229C= ENSP00000490508.1:p.Thr410=
ENST00000636471.1:c.1640C= ENSP00000490317.1:p.Thr547=
ENST00000636732.2:c.*1282C= ENSP00000490175.1:n.*1282C=
ENST00000636820.1:n.1665C=
ENST00000637045.1:c.1229C= ENSP00000490141.1:p.Thr410=
ENST00000637267.2:c.1565C= ENSP00000490293.2:p.Thr522=
ENST00000637304.1:c.1229C= ENSP00000490872.1:p.Thr410=
ENST00000638007.1:c.1229C= ENSP00000490723.1:p.Thr410=
ENST00000638087.1:c.1229C= ENSP00000490673.1:p.Thr410=
ENST00000638128.1:c.788C= ENSP00000490934.1:p.Thr263=
ENST00000675069.1:c.-133-772C= ENSP00000502467.1:n.-133-772C=
ENST00000675145.1:n.2113C=
ENST00000303660.8:c.1562C= ENSP00000302501.4:p.Thr521=
ENST00000409487.7:c.1565C= ENSP00000386854.2:p.Thr522=
ENST00000419938.5:c.655+1577C= ENSP00000394777.2:n.655+1577C=
ENST00000427902.5:c.1652C= ENSP00000395496.2:p.Thr551=
ENST00000440875.5:c.1154-72C= ENSP00000475553.2:n.1154-72C=
ENST00000539609.7:c.1493C= ENSP00000443792.2:p.Thr498=
ENST00000558170.6:c.1565C= ENSP00000454157.1:p.Thr522=
ENST00000627532.2:c.1565C= ENSP00000487174.1:p.Thr522=
NM_001171653.1:c.1493C= NP_001165124.1:p.Thr498=
NM_014795.3:c.1565C= NP_055610.1:p.Thr522=
XM_006712881.2:c.1565C= XP_006712944.1:p.Thr522=
XM_006712882.2:c.1565C= XP_006712945.1:p.Thr522=
XM_011512231.1:c.1556C= XP_011510533.1:p.Thr519=
XM_011512232.1:c.1544C= XP_011510534.1:p.Thr515=
NM_014795.4:c.1565C= MANE Select NP_055610.1:p.Thr522=
NM_001171653.2:c.1493C= NP_001165124.1:p.Thr498=