Canonical Allele Identifier: CA2586965034
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144404003_144404034del , CM000664.2:g.144404003_144404034del GRCh38
NC_000002.11:g.145161570_145161601del , CM000664.1:g.145161570_145161601del GRCh37
NC_000002.10:g.144878040_144878071del NCBI36
NG_016431.1:g.121359_121390del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*539_*570del ENSP00000508434.1:n.*539_*570del
ENST00000440875.6:c.-88_-57del ENSP00000475553.3:n.-88_-57del
ENST00000627532.3:c.690_721del MANE Select ENSP00000487174.1:p.Lys231PhefsTer6
ENST00000636026.2:c.690_721del ENSP00000490776.1:p.Lys231PhefsTer6
ENST00000636179.1:n.659_690del
ENST00000636413.1:c.354_385del ENSP00000490508.1:p.Lys119PhefsTer6
ENST00000636471.1:c.690_721del ENSP00000490317.1:p.Lys231PhefsTer6
ENST00000636732.2:c.*407_*438del ENSP00000490175.1:n.*407_*438del
ENST00000636820.1:n.790_821del
ENST00000637045.1:c.354_385del ENSP00000490141.1:p.Lys119PhefsTer6
ENST00000637267.2:c.690_721del ENSP00000490293.2:p.Lys231PhefsTer6
ENST00000637304.1:c.354_385del ENSP00000490872.1:p.Lys119PhefsTer6
ENST00000638007.1:c.354_385del ENSP00000490723.1:p.Lys119PhefsTer6
ENST00000638087.1:c.354_385del ENSP00000490673.1:p.Lys119PhefsTer6
ENST00000638128.1:c.-88_-57del ENSP00000490934.1:n.-88_-57del
ENST00000675069.1:c.-133-5183_-133-5152del ENSP00000502467.1:n.-133-5183_-133-5152del
ENST00000303660.8:c.687_718del ENSP00000302501.4:p.Lys230PhefsTer6
ENST00000392861.6:c.774_805del ENSP00000376601.3:p.Lys259PhefsTer6
ENST00000409487.7:c.690_721del ENSP00000386854.2:p.Lys231PhefsTer6
ENST00000419938.5:c.429_460del ENSP00000394777.2:p.Lys144PhefsTer6
ENST00000427902.5:c.777_808del ENSP00000395496.2:p.Lys260PhefsTer6
ENST00000440875.5:c.675_706del ENSP00000475553.2:p.Lys226PhefsTer6
ENST00000497268.1:n.636_667del
ENST00000539609.7:c.618_649del ENSP00000443792.2:p.Lys207PhefsTer6
ENST00000558170.6:c.690_721del ENSP00000454157.1:p.Lys231PhefsTer6
ENST00000627532.2:c.690_721del ENSP00000487174.1:p.Lys231PhefsTer6
NM_001171653.1:c.618_649del NP_001165124.1:p.Lys207PhefsTer6
NM_014795.3:c.690_721del NP_055610.1:p.Lys231PhefsTer6
XM_006712881.2:c.690_721del XP_006712944.1:p.Lys231PhefsTer6
XM_006712882.2:c.690_721del XP_006712945.1:p.Lys231PhefsTer6
XM_011512231.1:c.681_712del XP_011510533.1:p.Lys228PhefsTer6
XM_011512232.1:c.669_700del XP_011510534.1:p.Lys224PhefsTer6
NM_014795.4:c.690_721del MANE Select NP_055610.1:p.Lys231PhefsTer6
NM_001171653.2:c.618_649del NP_001165124.1:p.Lys207PhefsTer6