Canonical Allele Identifier: CA1294881319
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389746G= , CM000664.2:g.144389746G= GRCh38
NC_000002.11:g.145147313G= , CM000664.1:g.145147313G= GRCh37
NC_000002.10:g.144863783G= NCBI36
NG_016431.1:g.135646C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3199C= ENSP00000508434.1:n.*3199C=
ENST00000440875.6:c.2573C= ENSP00000475553.3:p.Thr858=
ENST00000627532.3:c.3350C= MANE Select ENSP00000487174.1:p.Thr1117=
ENST00000636026.2:c.3238C= ENSP00000490776.1:p.Pro1080=
ENST00000636179.1:n.3319C=
ENST00000636413.1:c.3014C= ENSP00000490508.1:p.Thr1005=
ENST00000636471.1:c.3425C= ENSP00000490317.1:p.Thr1142=
ENST00000636732.2:c.*3067C= ENSP00000490175.1:n.*3067C=
ENST00000636820.1:n.3450C=
ENST00000637045.1:c.3014C= ENSP00000490141.1:p.Thr1005=
ENST00000637304.1:c.3014C= ENSP00000490872.1:p.Thr1005=
ENST00000638007.1:c.3014C= ENSP00000490723.1:p.Thr1005=
ENST00000638087.1:c.3014C= ENSP00000490673.1:p.Thr1005=
ENST00000638128.1:c.2573C= ENSP00000490934.1:p.Thr858=
ENST00000639389.1:c.151+6666C= ENSP00000492572.1:n.151+6666C=
ENST00000647488.1:c.570C= ENSP00000494820.1:n.570C=
ENST00000675069.1:c.881C= ENSP00000502467.1:p.Thr294=
ENST00000303660.8:c.3347C= ENSP00000302501.4:p.Thr1116=
ENST00000409487.7:c.3350C= ENSP00000386854.2:p.Thr1117=
ENST00000419938.5:c.656-864C= ENSP00000394777.2:n.656-864C=
ENST00000539609.7:c.3278C= ENSP00000443792.2:p.Thr1093=
ENST00000558170.6:c.3350C= ENSP00000454157.1:p.Thr1117=
ENST00000627532.2:c.3350C= ENSP00000487174.1:p.Thr1117=
NM_001171653.1:c.3278C= NP_001165124.1:p.Thr1093=
NM_014795.3:c.3350C= NP_055610.1:p.Thr1117=
XM_006712881.2:c.3350C= XP_006712944.1:p.Thr1117=
XM_006712882.2:c.3350C= XP_006712945.1:p.Thr1117=
XM_011512231.1:c.3341C= XP_011510533.1:p.Thr1114=
XM_011512232.1:c.3329C= XP_011510534.1:p.Thr1110=
NM_014795.4:c.3350C= MANE Select NP_055610.1:p.Thr1117=
NM_001171653.2:c.3278C= NP_001165124.1:p.Thr1093=