Canonical Allele Identifier: CA2570644287

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399830_144399834del , CM000664.2:g.144399830_144399834del	GRCh38
NC_000002.11:g.145157397_145157401del , CM000664.1:g.145157397_145157401del	GRCh37
NC_000002.10:g.144873867_144873871del	NCBI36
NG_016431.1:g.125558_125562del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1202_*1206del	ENSP00000508434.1:n.*1202_*1206del
ENST00000440875.6:c.576_580del	ENSP00000475553.3:p.Thr193GlufsTer2
ENST00000627532.3:c.1353_1357del MANE Select	ENSP00000487174.1:p.Thr452GlufsTer2
ENST00000636026.2:c.1353_1357del	ENSP00000490776.1:p.Thr452GlufsTer2
ENST00000636179.1:n.1322_1326del
ENST00000636413.1:c.1017_1021del	ENSP00000490508.1:p.Thr340GlufsTer2
ENST00000636471.1:c.1428_1432del	ENSP00000490317.1:p.Thr477GlufsTer2
ENST00000636732.2:c.*1070_*1074del	ENSP00000490175.1:n.*1070_*1074del
ENST00000636820.1:n.1453_1457del
ENST00000637045.1:c.1017_1021del	ENSP00000490141.1:p.Thr340GlufsTer2
ENST00000637267.2:c.1353_1357del	ENSP00000490293.2:p.Thr452GlufsTer2
ENST00000637304.1:c.1017_1021del	ENSP00000490872.1:p.Thr340GlufsTer2
ENST00000638007.1:c.1017_1021del	ENSP00000490723.1:p.Thr340GlufsTer2
ENST00000638087.1:c.1017_1021del	ENSP00000490673.1:p.Thr340GlufsTer2
ENST00000638128.1:c.576_580del	ENSP00000490934.1:p.Thr193GlufsTer2
ENST00000675069.1:c.-133-984_-133-980del	ENSP00000502467.1:n.-133-984_-133-980del
ENST00000675145.1:n.1901_1905del
ENST00000303660.8:c.1350_1354del	ENSP00000302501.4:p.Thr451GlufsTer2
ENST00000409487.7:c.1353_1357del	ENSP00000386854.2:p.Thr452GlufsTer2
ENST00000419938.5:c.655+1365_655+1369del	ENSP00000394777.2:n.655+1365_655+1369del
ENST00000427902.5:c.1440_1444del	ENSP00000395496.2:p.Thr481GlufsTer2
ENST00000440875.5:c.1153+185_1153+189del	ENSP00000475553.2:n.1153+185_1153+189del
ENST00000539609.7:c.1281_1285del	ENSP00000443792.2:p.Thr428GlufsTer2
ENST00000558170.6:c.1353_1357del	ENSP00000454157.1:p.Thr452GlufsTer2
ENST00000627532.2:c.1353_1357del	ENSP00000487174.1:p.Thr452GlufsTer2
NM_001171653.1:c.1281_1285del	NP_001165124.1:p.Thr428GlufsTer2
NM_014795.3:c.1353_1357del	NP_055610.1:p.Thr452GlufsTer2
XM_006712881.2:c.1353_1357del	XP_006712944.1:p.Thr452GlufsTer2
XM_006712882.2:c.1353_1357del	XP_006712945.1:p.Thr452GlufsTer2
XM_011512231.1:c.1344_1348del	XP_011510533.1:p.Thr449GlufsTer2
XM_011512232.1:c.1332_1336del	XP_011510534.1:p.Thr445GlufsTer2
NM_014795.4:c.1353_1357del MANE Select	NP_055610.1:p.Thr452GlufsTer2
NM_001171653.2:c.1281_1285del	NP_001165124.1:p.Thr428GlufsTer2