Canonical Allele Identifier: CA348714701
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144403984T>A , CM000664.2:g.144403984T>A GRCh38
NC_000002.11:g.145161551T>A , CM000664.1:g.145161551T>A GRCh37
NC_000002.10:g.144878021T>A NCBI36
NG_016431.1:g.121408A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*588A>T ENSP00000508434.1:n.*588A>T
ENST00000440875.6:c.-39A>T ENSP00000475553.3:n.-39A>T
ENST00000627532.3:c.739A>T MANE Select ENSP00000487174.1:p.Ser247Cys
ENST00000636026.2:c.739A>T ENSP00000490776.1:p.Ser247Cys
ENST00000636179.1:n.708A>T
ENST00000636413.1:c.403A>T ENSP00000490508.1:p.Ser135Cys
ENST00000636471.1:c.739A>T ENSP00000490317.1:p.Ser247Cys
ENST00000636732.2:c.*456A>T ENSP00000490175.1:n.*456A>T
ENST00000636820.1:n.839A>T
ENST00000637045.1:c.403A>T ENSP00000490141.1:p.Ser135Cys
ENST00000637267.2:c.739A>T ENSP00000490293.2:p.Ser247Cys
ENST00000637304.1:c.403A>T ENSP00000490872.1:p.Ser135Cys
ENST00000638007.1:c.403A>T ENSP00000490723.1:p.Ser135Cys
ENST00000638087.1:c.403A>T ENSP00000490673.1:p.Ser135Cys
ENST00000638128.1:c.-39A>T ENSP00000490934.1:n.-39A>T
ENST00000675069.1:c.-133-5134A>T ENSP00000502467.1:n.-133-5134A>T
ENST00000303660.8:c.736A>T ENSP00000302501.4:p.Ser246Cys
ENST00000392861.6:c.823A>T ENSP00000376601.3:p.Ser275Cys
ENST00000409487.7:c.739A>T ENSP00000386854.2:p.Ser247Cys
ENST00000419938.5:c.478A>T ENSP00000394777.2:p.Ser160Cys
ENST00000427902.5:c.826A>T ENSP00000395496.2:p.Ser276Cys
ENST00000440875.5:c.724A>T ENSP00000475553.2:p.Ser242Cys
ENST00000539609.7:c.667A>T ENSP00000443792.2:p.Ser223Cys
ENST00000558170.6:c.739A>T ENSP00000454157.1:p.Ser247Cys
ENST00000627532.2:c.739A>T ENSP00000487174.1:p.Ser247Cys
NM_001171653.1:c.667A>T NP_001165124.1:p.Ser223Cys
NM_014795.3:c.739A>T NP_055610.1:p.Ser247Cys
XM_006712881.2:c.739A>T XP_006712944.1:p.Ser247Cys
XM_006712882.2:c.739A>T XP_006712945.1:p.Ser247Cys
XM_011512231.1:c.730A>T XP_011510533.1:p.Ser244Cys
XM_011512232.1:c.718A>T XP_011510534.1:p.Ser240Cys
NM_014795.4:c.739A>T MANE Select NP_055610.1:p.Ser247Cys
NM_001171653.2:c.667A>T NP_001165124.1:p.Ser223Cys