Canonical Allele Identifier: CA348714823
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144404035T>A , CM000664.2:g.144404035T>A GRCh38
NC_000002.11:g.145161602T>A , CM000664.1:g.145161602T>A GRCh37
NC_000002.10:g.144878072T>A NCBI36
NG_016431.1:g.121357A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*537A>T ENSP00000508434.1:n.*537A>T
ENST00000440875.6:c.-90A>T ENSP00000475553.3:n.-90A>T
ENST00000627532.3:c.688A>T MANE Select ENSP00000487174.1:p.Ile230Phe
ENST00000636026.2:c.688A>T ENSP00000490776.1:p.Ile230Phe
ENST00000636179.1:n.657A>T
ENST00000636413.1:c.352A>T ENSP00000490508.1:p.Ile118Phe
ENST00000636471.1:c.688A>T ENSP00000490317.1:p.Ile230Phe
ENST00000636732.2:c.*405A>T ENSP00000490175.1:n.*405A>T
ENST00000636820.1:n.788A>T
ENST00000637045.1:c.352A>T ENSP00000490141.1:p.Ile118Phe
ENST00000637267.2:c.688A>T ENSP00000490293.2:p.Ile230Phe
ENST00000637304.1:c.352A>T ENSP00000490872.1:p.Ile118Phe
ENST00000638007.1:c.352A>T ENSP00000490723.1:p.Ile118Phe
ENST00000638087.1:c.352A>T ENSP00000490673.1:p.Ile118Phe
ENST00000638128.1:c.-90A>T ENSP00000490934.1:n.-90A>T
ENST00000675069.1:c.-133-5185A>T ENSP00000502467.1:n.-133-5185A>T
ENST00000303660.8:c.685A>T ENSP00000302501.4:p.Ile229Phe
ENST00000392861.6:c.772A>T ENSP00000376601.3:p.Ile258Phe
ENST00000409487.7:c.688A>T ENSP00000386854.2:p.Ile230Phe
ENST00000419938.5:c.427A>T ENSP00000394777.2:p.Ile143Phe
ENST00000427902.5:c.775A>T ENSP00000395496.2:p.Ile259Phe
ENST00000440875.5:c.673A>T ENSP00000475553.2:p.Ile225Phe
ENST00000497268.1:n.634A>T
ENST00000539609.7:c.616A>T ENSP00000443792.2:p.Ile206Phe
ENST00000558170.6:c.688A>T ENSP00000454157.1:p.Ile230Phe
ENST00000627532.2:c.688A>T ENSP00000487174.1:p.Ile230Phe
NM_001171653.1:c.616A>T NP_001165124.1:p.Ile206Phe
NM_014795.3:c.688A>T NP_055610.1:p.Ile230Phe
XM_006712881.2:c.688A>T XP_006712944.1:p.Ile230Phe
XM_006712882.2:c.688A>T XP_006712945.1:p.Ile230Phe
XM_011512231.1:c.679A>T XP_011510533.1:p.Ile227Phe
XM_011512232.1:c.667A>T XP_011510534.1:p.Ile223Phe
NM_014795.4:c.688A>T MANE Select NP_055610.1:p.Ile230Phe
NM_001171653.2:c.616A>T NP_001165124.1:p.Ile206Phe