Canonical Allele Identifier: CA274520
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144429867_144429873del , CM000664.2:g.144429867_144429873del GRCh38
NC_000002.11:g.145187434_145187440del , CM000664.1:g.145187434_145187440del GRCh37
NC_000002.10:g.144903904_144903910del NCBI36
NG_016431.1:g.95519_95525del

Transcript Alleles

HGVS Amino-acid Change
ENST00000637591.2:n.376_382del
ENST00000689298.1:c.*148_*154del ENSP00000508434.1:n.*148_*154del
ENST00000440875.6:c.-479_-473del ENSP00000475553.3:n.-479_-473del
ENST00000627532.3:c.227_233del MANE Select ENSP00000487174.1:p.Gln76ArgfsTer11
ENST00000636026.2:c.227_233del ENSP00000490776.1:p.Gln76ArgfsTer11
ENST00000636179.1:n.196_202del
ENST00000636413.1:c.-110_-104del ENSP00000490508.1:n.-110_-104del
ENST00000636471.1:c.227_233del ENSP00000490317.1:p.Gln76ArgfsTer11
ENST00000636732.2:c.227_233del ENSP00000490175.1:p.Gln76ArgfsTer11
ENST00000636820.1:n.327_333del
ENST00000637045.1:c.-110_-104del ENSP00000490141.1:n.-110_-104del
ENST00000637267.2:c.227_233del ENSP00000490293.2:p.Gln76ArgfsTer11
ENST00000637304.1:c.-110_-104del ENSP00000490872.1:n.-110_-104del
ENST00000638007.1:c.-110_-104del ENSP00000490723.1:n.-110_-104del
ENST00000638087.1:c.-110_-104del ENSP00000490673.1:n.-110_-104del
ENST00000638128.1:c.-479_-473del ENSP00000490934.1:n.-479_-473del
ENST00000675069.1:c.-133-31023_-133-31017del ENSP00000502467.1:n.-133-31023_-133-31017del
ENST00000303660.8:c.227_233del ENSP00000302501.4:p.Gln76ArgfsTer11
ENST00000392861.6:c.311_317del ENSP00000376601.3:p.Gln104ArgfsTer11
ENST00000409211.5:c.227_233del ENSP00000387256.2:p.Gln76ArgfsTer11
ENST00000409487.7:c.227_233del ENSP00000386854.2:p.Gln76ArgfsTer11
ENST00000419938.5:c.227_233del ENSP00000394777.2:p.Gln76ArgfsTer11
ENST00000427902.5:c.314_320del ENSP00000395496.2:p.Gln105ArgfsTer11
ENST00000431672.4:c.227_233del ENSP00000475267.2:p.Gln76ArgfsTer11
ENST00000434448.5:c.*158_*164del ENSP00000487261.1:n.*158_*164del
ENST00000435831.5:c.227_233del ENSP00000400993.1:p.Gln76ArgfsTer11
ENST00000440875.5:c.212_218del ENSP00000475553.2:p.Gln71ArgfsTer11
ENST00000453352.5:n.534_540del
ENST00000461784.3:n.434_440del
ENST00000465308.5:c.227_233del ENSP00000487476.1:p.Gln76ArgfsTer11
ENST00000472146.5:n.477_483del
ENST00000476394.5:n.331_337del
ENST00000479735.1:n.458_464del
ENST00000539609.7:c.227_233del ENSP00000443792.2:p.Gln76ArgfsTer11
ENST00000558170.6:c.227_233del ENSP00000454157.1:p.Gln76ArgfsTer11
ENST00000627532.2:c.227_233del ENSP00000487174.1:p.Gln76ArgfsTer11
ENST00000627856.2:n.187_193del
NM_001171653.1:c.227_233del NP_001165124.1:p.Gln76ArgfsTer11
NM_014795.3:c.227_233del NP_055610.1:p.Gln76ArgfsTer11
XM_006712881.2:c.227_233del XP_006712944.1:p.Gln76ArgfsTer11
XM_006712882.2:c.227_233del XP_006712945.1:p.Gln76ArgfsTer11
XM_011512231.1:c.218_224del XP_011510533.1:p.Gln73ArgfsTer11
XM_011512232.1:c.206_212del XP_011510534.1:p.Gln69ArgfsTer11
NM_014795.4:c.227_233del MANE Select NP_055610.1:p.Gln76ArgfsTer11
NM_001171653.2:c.227_233del NP_001165124.1:p.Gln76ArgfsTer11