Canonical Allele Identifier: CA1294881252
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389561T= , CM000664.2:g.144389561T= GRCh38
NC_000002.11:g.145147128T= , CM000664.1:g.145147128T= GRCh37
NC_000002.10:g.144863598T= NCBI36
NG_016431.1:g.135831A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3384A= ENSP00000508434.1:n.*3384A=
ENST00000440875.6:c.2758A= ENSP00000475553.3:p.Ile920=
ENST00000627532.3:c.3535A= MANE Select ENSP00000487174.1:p.Ile1179=
ENST00000636026.2:c.3423A= ENSP00000490776.1:p.Arg1141=
ENST00000636179.1:n.3504A=
ENST00000636413.1:c.3199A= ENSP00000490508.1:p.Ile1067=
ENST00000636471.1:c.3610A= ENSP00000490317.1:p.Ile1204=
ENST00000636732.2:c.*3252A= ENSP00000490175.1:n.*3252A=
ENST00000636820.1:n.3635A=
ENST00000637045.1:c.3199A= ENSP00000490141.1:p.Ile1067=
ENST00000637304.1:c.3199A= ENSP00000490872.1:p.Ile1067=
ENST00000638007.1:c.3199A= ENSP00000490723.1:p.Ile1067=
ENST00000638087.1:c.3199A= ENSP00000490673.1:p.Ile1067=
ENST00000638128.1:c.2758A= ENSP00000490934.1:p.Ile920=
ENST00000639389.1:c.151+6851A= ENSP00000492572.1:n.151+6851A=
ENST00000647488.1:c.755A= ENSP00000494820.1:n.755A=
ENST00000675069.1:c.1066A= ENSP00000502467.1:p.Ile356=
ENST00000303660.8:c.3532A= ENSP00000302501.4:p.Ile1178=
ENST00000409487.7:c.3535A= ENSP00000386854.2:p.Ile1179=
ENST00000419938.5:c.656-679A= ENSP00000394777.2:n.656-679A=
ENST00000539609.7:c.3463A= ENSP00000443792.2:p.Ile1155=
ENST00000558170.6:c.3535A= ENSP00000454157.1:p.Ile1179=
ENST00000627532.2:c.3535A= ENSP00000487174.1:p.Ile1179=
NM_001171653.1:c.3463A= NP_001165124.1:p.Ile1155=
NM_014795.3:c.3535A= NP_055610.1:p.Ile1179=
XM_006712881.2:c.3535A= XP_006712944.1:p.Ile1179=
XM_006712882.2:c.3535A= XP_006712945.1:p.Ile1179=
XM_011512231.1:c.3526A= XP_011510533.1:p.Ile1176=
XM_011512232.1:c.3514A= XP_011510534.1:p.Ile1172=
NM_014795.4:c.3535A= MANE Select NP_055610.1:p.Ile1179=
NM_001171653.2:c.3463A= NP_001165124.1:p.Ile1155=