Canonical Allele Identifier: CA2586969975
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389567del , CM000664.2:g.144389567del GRCh38
NC_000002.11:g.145147134del , CM000664.1:g.145147134del GRCh37
NC_000002.10:g.144863604del NCBI36
NG_016431.1:g.135825del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3378del ENSP00000508434.1:n.*3378del
ENST00000440875.6:c.2752del ENSP00000475553.3:p.Glu918LysfsTer?
ENST00000627532.3:c.3529del MANE Select ENSP00000487174.1:p.Glu1177LysfsTer?
ENST00000636026.2:c.3417del ENSP00000490776.1:p.Lys1140AsnfsTer5
ENST00000636179.1:n.3498del
ENST00000636413.1:c.3193del ENSP00000490508.1:p.Glu1065LysfsTer?
ENST00000636471.1:c.3604del ENSP00000490317.1:p.Glu1202LysfsTer?
ENST00000636732.2:c.*3246del ENSP00000490175.1:n.*3246del
ENST00000636820.1:n.3629del
ENST00000637045.1:c.3193del ENSP00000490141.1:p.Glu1065LysfsTer?
ENST00000637304.1:c.3193del ENSP00000490872.1:p.Glu1065LysfsTer?
ENST00000638007.1:c.3193del ENSP00000490723.1:p.Glu1065LysfsTer?
ENST00000638087.1:c.3193del ENSP00000490673.1:p.Glu1065LysfsTer?
ENST00000638128.1:c.2752del ENSP00000490934.1:p.Glu918LysfsTer?
ENST00000639389.1:c.151+6845del ENSP00000492572.1:n.151+6845del
ENST00000647488.1:c.749del ENSP00000494820.1:n.749del
ENST00000675069.1:c.1060del ENSP00000502467.1:p.Glu354LysfsTer?
ENST00000303660.8:c.3526del ENSP00000302501.4:p.Glu1176LysfsTer?
ENST00000409487.7:c.3529del ENSP00000386854.2:p.Glu1177LysfsTer?
ENST00000419938.5:c.656-685del ENSP00000394777.2:n.656-685del
ENST00000539609.7:c.3457del ENSP00000443792.2:p.Glu1153LysfsTer?
ENST00000558170.6:c.3529del ENSP00000454157.1:p.Glu1177LysfsTer?
ENST00000627532.2:c.3529del ENSP00000487174.1:p.Glu1177LysfsTer?
NM_001171653.1:c.3457del NP_001165124.1:p.Glu1153LysfsTer?
NM_014795.3:c.3529del NP_055610.1:p.Glu1177LysfsTer?
XM_006712881.2:c.3529del XP_006712944.1:p.Glu1177LysfsTer?
XM_006712882.2:c.3529del XP_006712945.1:p.Glu1177LysfsTer?
XM_011512231.1:c.3520del XP_011510533.1:p.Glu1174LysfsTer?
XM_011512232.1:c.3508del XP_011510534.1:p.Glu1170LysfsTer?
NM_014795.4:c.3529del MANE Select NP_055610.1:p.Glu1177LysfsTer?
NM_001171653.2:c.3457del NP_001165124.1:p.Glu1153LysfsTer?