Canonical Allele Identifier: CA2586970129

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399820_144399821insA , CM000664.2:g.144399820_144399821insA	GRCh38
NC_000002.11:g.145157387_145157388insA , CM000664.1:g.145157387_145157388insA	GRCh37
NC_000002.10:g.144873857_144873858insA	NCBI36
NG_016431.1:g.125571_125572insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1215_*1216insT	ENSP00000508434.1:n.*1215_*1216insT
ENST00000440875.6:c.589_590insT	ENSP00000475553.3:p.Asn197IlefsTer4
ENST00000627532.3:c.1366_1367insT MANE Select	ENSP00000487174.1:p.Asn456IlefsTer4
ENST00000636026.2:c.1366_1367insT	ENSP00000490776.1:p.Asn456IlefsTer4
ENST00000636179.1:n.1335_1336insT
ENST00000636413.1:c.1030_1031insT	ENSP00000490508.1:p.Asn344IlefsTer4
ENST00000636471.1:c.1441_1442insT	ENSP00000490317.1:p.Asn481IlefsTer4
ENST00000636732.2:c.*1083_*1084insT	ENSP00000490175.1:n.*1083_*1084insT
ENST00000636820.1:n.1466_1467insT
ENST00000637045.1:c.1030_1031insT	ENSP00000490141.1:p.Asn344IlefsTer4
ENST00000637267.2:c.1366_1367insT	ENSP00000490293.2:p.Asn456IlefsTer4
ENST00000637304.1:c.1030_1031insT	ENSP00000490872.1:p.Asn344IlefsTer4
ENST00000638007.1:c.1030_1031insT	ENSP00000490723.1:p.Asn344IlefsTer4
ENST00000638087.1:c.1030_1031insT	ENSP00000490673.1:p.Asn344IlefsTer4
ENST00000638128.1:c.589_590insT	ENSP00000490934.1:p.Asn197IlefsTer4
ENST00000675069.1:c.-133-971_-133-970insT	ENSP00000502467.1:n.-133-971_-133-970insT
ENST00000675145.1:n.1914_1915insT
ENST00000303660.8:c.1363_1364insT	ENSP00000302501.4:p.Asn455IlefsTer4
ENST00000409487.7:c.1366_1367insT	ENSP00000386854.2:p.Asn456IlefsTer4
ENST00000419938.5:c.655+1378_655+1379insT	ENSP00000394777.2:n.655+1378_655+1379insT
ENST00000427902.5:c.1453_1454insT	ENSP00000395496.2:p.Asn485IlefsTer4
ENST00000440875.5:c.1153+198_1153+199insT	ENSP00000475553.2:n.1153+198_1153+199insT
ENST00000539609.7:c.1294_1295insT	ENSP00000443792.2:p.Asn432IlefsTer4
ENST00000558170.6:c.1366_1367insT	ENSP00000454157.1:p.Asn456IlefsTer4
ENST00000627532.2:c.1366_1367insT	ENSP00000487174.1:p.Asn456IlefsTer4
NM_001171653.1:c.1294_1295insT	NP_001165124.1:p.Asn432IlefsTer4
NM_014795.3:c.1366_1367insT	NP_055610.1:p.Asn456IlefsTer4
XM_006712881.2:c.1366_1367insT	XP_006712944.1:p.Asn456IlefsTer4
XM_006712882.2:c.1366_1367insT	XP_006712945.1:p.Asn456IlefsTer4
XM_011512231.1:c.1357_1358insT	XP_011510533.1:p.Asn453IlefsTer4
XM_011512232.1:c.1345_1346insT	XP_011510534.1:p.Asn449IlefsTer4
NM_014795.4:c.1366_1367insT MANE Select	NP_055610.1:p.Asn456IlefsTer4
NM_001171653.2:c.1294_1295insT	NP_001165124.1:p.Asn432IlefsTer4