Canonical Allele Identifier: CA1294884959
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398592G= , CM000664.2:g.144398592G= GRCh38
NC_000002.11:g.145156159G= , CM000664.1:g.145156159G= GRCh37
NC_000002.10:g.144872629G= NCBI36
NG_016431.1:g.126800C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2444C= ENSP00000508434.1:n.*2444C=
ENST00000440875.6:c.1818C= ENSP00000475553.3:p.Ile606=
ENST00000627532.3:c.2595C= MANE Select ENSP00000487174.1:p.Ile865=
ENST00000636026.2:c.2595C= ENSP00000490776.1:p.Ile865=
ENST00000636179.1:n.2564C=
ENST00000636413.1:c.2259C= ENSP00000490508.1:p.Ile753=
ENST00000636471.1:c.2670C= ENSP00000490317.1:p.Ile890=
ENST00000636732.2:c.*2312C= ENSP00000490175.1:n.*2312C=
ENST00000636820.1:n.2695C=
ENST00000637045.1:c.2259C= ENSP00000490141.1:p.Ile753=
ENST00000637304.1:c.2259C= ENSP00000490872.1:p.Ile753=
ENST00000638007.1:c.2259C= ENSP00000490723.1:p.Ile753=
ENST00000638087.1:c.2259C= ENSP00000490673.1:p.Ile753=
ENST00000638128.1:c.1818C= ENSP00000490934.1:p.Ile606=
ENST00000675069.1:c.126C= ENSP00000502467.1:p.Ile42=
ENST00000303660.8:c.2592C= ENSP00000302501.4:p.Ile864=
ENST00000409487.7:c.2595C= ENSP00000386854.2:p.Ile865=
ENST00000419938.5:c.655+2607C= ENSP00000394777.2:n.655+2607C=
ENST00000440875.5:c.1168-664C= ENSP00000475553.2:n.1168-664C=
ENST00000539609.7:c.2523C= ENSP00000443792.2:p.Ile841=
ENST00000558170.6:c.2595C= ENSP00000454157.1:p.Ile865=
ENST00000627532.2:c.2595C= ENSP00000487174.1:p.Ile865=
NM_001171653.1:c.2523C= NP_001165124.1:p.Ile841=
NM_014795.3:c.2595C= NP_055610.1:p.Ile865=
XM_006712881.2:c.2595C= XP_006712944.1:p.Ile865=
XM_006712882.2:c.2595C= XP_006712945.1:p.Ile865=
XM_011512231.1:c.2586C= XP_011510533.1:p.Ile862=
XM_011512232.1:c.2574C= XP_011510534.1:p.Ile858=
NM_014795.4:c.2595C= MANE Select NP_055610.1:p.Ile865=
NM_001171653.2:c.2523C= NP_001165124.1:p.Ile841=