Canonical Allele Identifier: CA1294881279
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389641C= , CM000664.2:g.144389641C= GRCh38
NC_000002.11:g.145147208C= , CM000664.1:g.145147208C= GRCh37
NC_000002.10:g.144863678C= NCBI36
NG_016431.1:g.135751G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3304G= ENSP00000508434.1:n.*3304G=
ENST00000440875.6:c.2678G= ENSP00000475553.3:p.Gly893=
ENST00000627532.3:c.3455G= MANE Select ENSP00000487174.1:p.Gly1152=
ENST00000636026.2:c.3343G= ENSP00000490776.1:p.Ala1115=
ENST00000636179.1:n.3424G=
ENST00000636413.1:c.3119G= ENSP00000490508.1:p.Gly1040=
ENST00000636471.1:c.3530G= ENSP00000490317.1:p.Gly1177=
ENST00000636732.2:c.*3172G= ENSP00000490175.1:n.*3172G=
ENST00000636820.1:n.3555G=
ENST00000637045.1:c.3119G= ENSP00000490141.1:p.Gly1040=
ENST00000637304.1:c.3119G= ENSP00000490872.1:p.Gly1040=
ENST00000638007.1:c.3119G= ENSP00000490723.1:p.Gly1040=
ENST00000638087.1:c.3119G= ENSP00000490673.1:p.Gly1040=
ENST00000638128.1:c.2678G= ENSP00000490934.1:p.Gly893=
ENST00000639389.1:c.151+6771G= ENSP00000492572.1:n.151+6771G=
ENST00000647488.1:c.675G= ENSP00000494820.1:n.675G=
ENST00000675069.1:c.986G= ENSP00000502467.1:p.Gly329=
ENST00000303660.8:c.3452G= ENSP00000302501.4:p.Gly1151=
ENST00000409487.7:c.3455G= ENSP00000386854.2:p.Gly1152=
ENST00000419938.5:c.656-759G= ENSP00000394777.2:n.656-759G=
ENST00000539609.7:c.3383G= ENSP00000443792.2:p.Gly1128=
ENST00000558170.6:c.3455G= ENSP00000454157.1:p.Gly1152=
ENST00000627532.2:c.3455G= ENSP00000487174.1:p.Gly1152=
NM_001171653.1:c.3383G= NP_001165124.1:p.Gly1128=
NM_014795.3:c.3455G= NP_055610.1:p.Gly1152=
XM_006712881.2:c.3455G= XP_006712944.1:p.Gly1152=
XM_006712882.2:c.3455G= XP_006712945.1:p.Gly1152=
XM_011512231.1:c.3446G= XP_011510533.1:p.Gly1149=
XM_011512232.1:c.3434G= XP_011510534.1:p.Gly1145=
NM_014795.4:c.3455G= MANE Select NP_055610.1:p.Gly1152=
NM_001171653.2:c.3383G= NP_001165124.1:p.Gly1128=