Canonical Allele Identifier: CA2586970132
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399866_144399870del , CM000664.2:g.144399866_144399870del GRCh38
NC_000002.11:g.145157433_145157437del , CM000664.1:g.145157433_145157437del GRCh37
NC_000002.10:g.144873903_144873907del NCBI36
NG_016431.1:g.125522_125526del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1166_*1170del ENSP00000508434.1:n.*1166_*1170del
ENST00000440875.6:c.540_544del ENSP00000475553.3:p.Leu180PhefsTer15
ENST00000627532.3:c.1317_1321del MANE Select ENSP00000487174.1:p.Leu439PhefsTer15
ENST00000636026.2:c.1317_1321del ENSP00000490776.1:p.Leu439PhefsTer15
ENST00000636179.1:n.1286_1290del
ENST00000636413.1:c.981_985del ENSP00000490508.1:p.Leu327PhefsTer15
ENST00000636471.1:c.1392_1396del ENSP00000490317.1:p.Leu464PhefsTer15
ENST00000636732.2:c.*1034_*1038del ENSP00000490175.1:n.*1034_*1038del
ENST00000636820.1:n.1417_1421del
ENST00000637045.1:c.981_985del ENSP00000490141.1:p.Leu327PhefsTer15
ENST00000637267.2:c.1317_1321del ENSP00000490293.2:p.Leu439PhefsTer15
ENST00000637304.1:c.981_985del ENSP00000490872.1:p.Leu327PhefsTer15
ENST00000638007.1:c.981_985del ENSP00000490723.1:p.Leu327PhefsTer15
ENST00000638087.1:c.981_985del ENSP00000490673.1:p.Leu327PhefsTer15
ENST00000638128.1:c.540_544del ENSP00000490934.1:p.Leu180PhefsTer15
ENST00000675069.1:c.-133-1020_-133-1016del ENSP00000502467.1:n.-133-1020_-133-1016del
ENST00000675145.1:n.1865_1869del
ENST00000303660.8:c.1314_1318del ENSP00000302501.4:p.Leu438PhefsTer15
ENST00000409487.7:c.1317_1321del ENSP00000386854.2:p.Leu439PhefsTer15
ENST00000419938.5:c.655+1329_655+1333del ENSP00000394777.2:n.655+1329_655+1333del
ENST00000427902.5:c.1404_1408del ENSP00000395496.2:p.Leu468PhefsTer15
ENST00000440875.5:c.1153+149_1153+153del ENSP00000475553.2:n.1153+149_1153+153del
ENST00000539609.7:c.1245_1249del ENSP00000443792.2:p.Leu415PhefsTer15
ENST00000558170.6:c.1317_1321del ENSP00000454157.1:p.Leu439PhefsTer15
ENST00000627532.2:c.1317_1321del ENSP00000487174.1:p.Leu439PhefsTer15
NM_001171653.1:c.1245_1249del NP_001165124.1:p.Leu415PhefsTer15
NM_014795.3:c.1317_1321del NP_055610.1:p.Leu439PhefsTer15
XM_006712881.2:c.1317_1321del XP_006712944.1:p.Leu439PhefsTer15
XM_006712882.2:c.1317_1321del XP_006712945.1:p.Leu439PhefsTer15
XM_011512231.1:c.1308_1312del XP_011510533.1:p.Leu436PhefsTer15
XM_011512232.1:c.1296_1300del XP_011510534.1:p.Leu432PhefsTer15
NM_014795.4:c.1317_1321del MANE Select NP_055610.1:p.Leu439PhefsTer15
NM_001171653.2:c.1245_1249del NP_001165124.1:p.Leu415PhefsTer15