Canonical Allele Identifier: CA1294885022
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398769G= , CM000664.2:g.144398769G= GRCh38
NC_000002.11:g.145156336G= , CM000664.1:g.145156336G= GRCh37
NC_000002.10:g.144872806G= NCBI36
NG_016431.1:g.126623C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2267C= ENSP00000508434.1:n.*2267C=
ENST00000440875.6:c.1641C= ENSP00000475553.3:p.Phe547=
ENST00000627532.3:c.2418C= MANE Select ENSP00000487174.1:p.Phe806=
ENST00000636026.2:c.2418C= ENSP00000490776.1:p.Phe806=
ENST00000636179.1:n.2387C=
ENST00000636413.1:c.2082C= ENSP00000490508.1:p.Phe694=
ENST00000636471.1:c.2493C= ENSP00000490317.1:p.Phe831=
ENST00000636732.2:c.*2135C= ENSP00000490175.1:n.*2135C=
ENST00000636820.1:n.2518C=
ENST00000637045.1:c.2082C= ENSP00000490141.1:p.Phe694=
ENST00000637304.1:c.2082C= ENSP00000490872.1:p.Phe694=
ENST00000638007.1:c.2082C= ENSP00000490723.1:p.Phe694=
ENST00000638087.1:c.2082C= ENSP00000490673.1:p.Phe694=
ENST00000638128.1:c.1641C= ENSP00000490934.1:p.Phe547=
ENST00000675069.1:c.-52C= ENSP00000502467.1:n.-52C=
ENST00000675145.1:n.2966C=
ENST00000303660.8:c.2415C= ENSP00000302501.4:p.Phe805=
ENST00000409487.7:c.2418C= ENSP00000386854.2:p.Phe806=
ENST00000419938.5:c.655+2430C= ENSP00000394777.2:n.655+2430C=
ENST00000440875.5:c.1167+768C= ENSP00000475553.2:n.1167+768C=
ENST00000539609.7:c.2346C= ENSP00000443792.2:p.Phe782=
ENST00000558170.6:c.2418C= ENSP00000454157.1:p.Phe806=
ENST00000627532.2:c.2418C= ENSP00000487174.1:p.Phe806=
NM_001171653.1:c.2346C= NP_001165124.1:p.Phe782=
NM_014795.3:c.2418C= NP_055610.1:p.Phe806=
XM_006712881.2:c.2418C= XP_006712944.1:p.Phe806=
XM_006712882.2:c.2418C= XP_006712945.1:p.Phe806=
XM_011512231.1:c.2409C= XP_011510533.1:p.Phe803=
XM_011512232.1:c.2397C= XP_011510534.1:p.Phe799=
NM_014795.4:c.2418C= MANE Select NP_055610.1:p.Phe806=
NM_001171653.2:c.2346C= NP_001165124.1:p.Phe782=