Canonical Allele Identifier: CA1294881361
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389832C= , CM000664.2:g.144389832C= GRCh38
NC_000002.11:g.145147399C= , CM000664.1:g.145147399C= GRCh37
NC_000002.10:g.144863869C= NCBI36
NG_016431.1:g.135560G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3113G= ENSP00000508434.1:n.*3113G=
ENST00000440875.6:c.2487G= ENSP00000475553.3:p.Arg829=
ENST00000627532.3:c.3264G= MANE Select ENSP00000487174.1:p.Arg1088=
ENST00000636026.2:c.3230+34G= ENSP00000490776.1:n.3230+34G=
ENST00000636179.1:n.3233G=
ENST00000636413.1:c.2928G= ENSP00000490508.1:p.Arg976=
ENST00000636471.1:c.3339G= ENSP00000490317.1:p.Arg1113=
ENST00000636732.2:c.*2981G= ENSP00000490175.1:n.*2981G=
ENST00000636820.1:n.3364G=
ENST00000637045.1:c.2928G= ENSP00000490141.1:p.Arg976=
ENST00000637304.1:c.2928G= ENSP00000490872.1:p.Arg976=
ENST00000638007.1:c.2928G= ENSP00000490723.1:p.Arg976=
ENST00000638087.1:c.2928G= ENSP00000490673.1:p.Arg976=
ENST00000638128.1:c.2487G= ENSP00000490934.1:p.Arg829=
ENST00000639389.1:c.151+6580G= ENSP00000492572.1:n.151+6580G=
ENST00000647488.1:c.484G= ENSP00000494820.1:n.484G=
ENST00000675069.1:c.795G= ENSP00000502467.1:p.Arg265=
ENST00000303660.8:c.3261G= ENSP00000302501.4:p.Arg1087=
ENST00000409487.7:c.3264G= ENSP00000386854.2:p.Arg1088=
ENST00000419938.5:c.656-950G= ENSP00000394777.2:n.656-950G=
ENST00000539609.7:c.3192G= ENSP00000443792.2:p.Arg1064=
ENST00000558170.6:c.3264G= ENSP00000454157.1:p.Arg1088=
ENST00000627532.2:c.3264G= ENSP00000487174.1:p.Arg1088=
NM_001171653.1:c.3192G= NP_001165124.1:p.Arg1064=
NM_014795.3:c.3264G= NP_055610.1:p.Arg1088=
XM_006712881.2:c.3264G= XP_006712944.1:p.Arg1088=
XM_006712882.2:c.3264G= XP_006712945.1:p.Arg1088=
XM_011512231.1:c.3255G= XP_011510533.1:p.Arg1085=
XM_011512232.1:c.3243G= XP_011510534.1:p.Arg1081=
NM_014795.4:c.3264G= MANE Select NP_055610.1:p.Arg1088=
NM_001171653.2:c.3192G= NP_001165124.1:p.Arg1064=