Canonical Allele Identifier: CA429445998
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399818_144399822del , CM000664.2:g.144399818_144399822del GRCh38
NC_000002.11:g.145157385_145157389del , CM000664.1:g.145157385_145157389del GRCh37
NC_000002.10:g.144873855_144873859del NCBI36
NG_016431.1:g.125573_125577del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1217_*1221del ENSP00000508434.1:n.*1217_*1221del
ENST00000440875.6:c.591_595del ENSP00000475553.3:p.Asn197LysfsTer2
ENST00000627532.3:c.1368_1372del MANE Select ENSP00000487174.1:p.Asn456LysfsTer2
ENST00000636026.2:c.1368_1372del ENSP00000490776.1:p.Asn456LysfsTer2
ENST00000636179.1:n.1337_1341del
ENST00000636413.1:c.1032_1036del ENSP00000490508.1:p.Asn344LysfsTer2
ENST00000636471.1:c.1443_1447del ENSP00000490317.1:p.Asn481LysfsTer2
ENST00000636732.2:c.*1085_*1089del ENSP00000490175.1:n.*1085_*1089del
ENST00000636820.1:n.1468_1472del
ENST00000637045.1:c.1032_1036del ENSP00000490141.1:p.Asn344LysfsTer2
ENST00000637267.2:c.1368_1372del ENSP00000490293.2:p.Asn456LysfsTer2
ENST00000637304.1:c.1032_1036del ENSP00000490872.1:p.Asn344LysfsTer2
ENST00000638007.1:c.1032_1036del ENSP00000490723.1:p.Asn344LysfsTer2
ENST00000638087.1:c.1032_1036del ENSP00000490673.1:p.Asn344LysfsTer2
ENST00000638128.1:c.591_595del ENSP00000490934.1:p.Asn197LysfsTer2
ENST00000675069.1:c.-133-969_-133-965del ENSP00000502467.1:n.-133-969_-133-965del
ENST00000675145.1:n.1916_1920del
ENST00000303660.8:c.1365_1369del ENSP00000302501.4:p.Asn455LysfsTer2
ENST00000409487.7:c.1368_1372del ENSP00000386854.2:p.Asn456LysfsTer2
ENST00000419938.5:c.655+1380_655+1384del ENSP00000394777.2:n.655+1380_655+1384del
ENST00000427902.5:c.1455_1459del ENSP00000395496.2:p.Asn485LysfsTer2
ENST00000440875.5:c.1153+200_1153+204del ENSP00000475553.2:n.1153+200_1153+204del
ENST00000539609.7:c.1296_1300del ENSP00000443792.2:p.Asn432LysfsTer2
ENST00000558170.6:c.1368_1372del ENSP00000454157.1:p.Asn456LysfsTer2
ENST00000627532.2:c.1368_1372del ENSP00000487174.1:p.Asn456LysfsTer2
NM_001171653.1:c.1296_1300del NP_001165124.1:p.Asn432LysfsTer2
NM_014795.3:c.1368_1372del NP_055610.1:p.Asn456LysfsTer2
XM_006712881.2:c.1368_1372del XP_006712944.1:p.Asn456LysfsTer2
XM_006712882.2:c.1368_1372del XP_006712945.1:p.Asn456LysfsTer2
XM_011512231.1:c.1359_1363del XP_011510533.1:p.Asn453LysfsTer2
XM_011512232.1:c.1347_1351del XP_011510534.1:p.Asn449LysfsTer2
NM_014795.4:c.1368_1372del MANE Select NP_055610.1:p.Asn456LysfsTer2
NM_001171653.2:c.1296_1300del NP_001165124.1:p.Asn432LysfsTer2