Canonical Allele Identifier: CA2586970139

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144400010_144400013del , CM000664.2:g.144400010_144400013del	GRCh38
NC_000002.11:g.145157577_145157580del , CM000664.1:g.145157577_145157580del	GRCh37
NC_000002.10:g.144874047_144874050del	NCBI36
NG_016431.1:g.125380_125383del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1024_*1027del	ENSP00000508434.1:n.*1024_*1027del
ENST00000440875.6:c.398_401del	ENSP00000475553.3:p.Thr133AsnfsTer3
ENST00000627532.3:c.1175_1178del MANE Select	ENSP00000487174.1:p.Thr392AsnfsTer3
ENST00000636026.2:c.1175_1178del	ENSP00000490776.1:p.Thr392AsnfsTer3
ENST00000636179.1:n.1144_1147del
ENST00000636413.1:c.839_842del	ENSP00000490508.1:p.Thr280AsnfsTer3
ENST00000636471.1:c.1250_1253del	ENSP00000490317.1:p.Thr417AsnfsTer3
ENST00000636732.2:c.*892_*895del	ENSP00000490175.1:n.*892_*895del
ENST00000636820.1:n.1275_1278del
ENST00000637045.1:c.839_842del	ENSP00000490141.1:p.Thr280AsnfsTer3
ENST00000637267.2:c.1175_1178del	ENSP00000490293.2:p.Thr392AsnfsTer3
ENST00000637304.1:c.839_842del	ENSP00000490872.1:p.Thr280AsnfsTer3
ENST00000638007.1:c.839_842del	ENSP00000490723.1:p.Thr280AsnfsTer3
ENST00000638087.1:c.839_842del	ENSP00000490673.1:p.Thr280AsnfsTer3
ENST00000638128.1:c.398_401del	ENSP00000490934.1:p.Thr133AsnfsTer3
ENST00000675069.1:c.-133-1162_-133-1159del	ENSP00000502467.1:n.-133-1162_-133-1159del
ENST00000675145.1:n.1723_1726del
ENST00000303660.8:c.1172_1175del	ENSP00000302501.4:p.Thr391AsnfsTer3
ENST00000392861.6:c.1259_1262del	ENSP00000376601.3:p.Thr420AsnfsTer3
ENST00000409487.7:c.1175_1178del	ENSP00000386854.2:p.Thr392AsnfsTer3
ENST00000419938.5:c.655+1187_655+1190del	ENSP00000394777.2:n.655+1187_655+1190del
ENST00000427902.5:c.1262_1265del	ENSP00000395496.2:p.Thr421AsnfsTer3
ENST00000440875.5:c.1153+7_1153+10del	ENSP00000475553.2:n.1153+7_1153+10del
ENST00000539609.7:c.1103_1106del	ENSP00000443792.2:p.Thr368AsnfsTer3
ENST00000558170.6:c.1175_1178del	ENSP00000454157.1:p.Thr392AsnfsTer3
ENST00000627532.2:c.1175_1178del	ENSP00000487174.1:p.Thr392AsnfsTer3
NM_001171653.1:c.1103_1106del	NP_001165124.1:p.Thr368AsnfsTer3
NM_014795.3:c.1175_1178del	NP_055610.1:p.Thr392AsnfsTer3
XM_006712881.2:c.1175_1178del	XP_006712944.1:p.Thr392AsnfsTer3
XM_006712882.2:c.1175_1178del	XP_006712945.1:p.Thr392AsnfsTer3
XM_011512231.1:c.1166_1169del	XP_011510533.1:p.Thr389AsnfsTer3
XM_011512232.1:c.1154_1157del	XP_011510534.1:p.Thr385AsnfsTer3
NM_014795.4:c.1175_1178del MANE Select	NP_055610.1:p.Thr392AsnfsTer3
NM_001171653.2:c.1103_1106del	NP_001165124.1:p.Thr368AsnfsTer3