Canonical Allele Identifier: CA1294885392
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399727T= , CM000664.2:g.144399727T= GRCh38
NC_000002.11:g.145157294T= , CM000664.1:g.145157294T= GRCh37
NC_000002.10:g.144873764T= NCBI36
NG_016431.1:g.125665A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1309A= ENSP00000508434.1:n.*1309A=
ENST00000440875.6:c.683A= ENSP00000475553.3:p.Lys228=
ENST00000627532.3:c.1460A= MANE Select ENSP00000487174.1:p.Lys487=
ENST00000636026.2:c.1460A= ENSP00000490776.1:p.Lys487=
ENST00000636179.1:n.1429A=
ENST00000636413.1:c.1124A= ENSP00000490508.1:p.Lys375=
ENST00000636471.1:c.1535A= ENSP00000490317.1:p.Lys512=
ENST00000636732.2:c.*1177A= ENSP00000490175.1:n.*1177A=
ENST00000636820.1:n.1560A=
ENST00000637045.1:c.1124A= ENSP00000490141.1:p.Lys375=
ENST00000637267.2:c.1460A= ENSP00000490293.2:p.Lys487=
ENST00000637304.1:c.1124A= ENSP00000490872.1:p.Lys375=
ENST00000638007.1:c.1124A= ENSP00000490723.1:p.Lys375=
ENST00000638087.1:c.1124A= ENSP00000490673.1:p.Lys375=
ENST00000638128.1:c.683A= ENSP00000490934.1:p.Lys228=
ENST00000675069.1:c.-133-877A= ENSP00000502467.1:n.-133-877A=
ENST00000675145.1:n.2008A=
ENST00000303660.8:c.1457A= ENSP00000302501.4:p.Lys486=
ENST00000409487.7:c.1460A= ENSP00000386854.2:p.Lys487=
ENST00000419938.5:c.655+1472A= ENSP00000394777.2:n.655+1472A=
ENST00000427902.5:c.1547A= ENSP00000395496.2:p.Lys516=
ENST00000440875.5:c.1154-177A= ENSP00000475553.2:n.1154-177A=
ENST00000539609.7:c.1388A= ENSP00000443792.2:p.Lys463=
ENST00000558170.6:c.1460A= ENSP00000454157.1:p.Lys487=
ENST00000627532.2:c.1460A= ENSP00000487174.1:p.Lys487=
NM_001171653.1:c.1388A= NP_001165124.1:p.Lys463=
NM_014795.3:c.1460A= NP_055610.1:p.Lys487=
XM_006712881.2:c.1460A= XP_006712944.1:p.Lys487=
XM_006712882.2:c.1460A= XP_006712945.1:p.Lys487=
XM_011512231.1:c.1451A= XP_011510533.1:p.Lys484=
XM_011512232.1:c.1439A= XP_011510534.1:p.Lys480=
NM_014795.4:c.1460A= MANE Select NP_055610.1:p.Lys487=
NM_001171653.2:c.1388A= NP_001165124.1:p.Lys463=