Canonical Allele Identifier: CA1294887176

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403961_144403963delinsGGT , CM000664.2:g.144403961_144403963delinsGGT	GRCh38
NC_000002.11:g.145161528_145161530delinsGGT , CM000664.1:g.145161528_145161530delinsGGT	GRCh37
NC_000002.10:g.144877998_144878000delinsGGT	NCBI36
NG_016431.1:g.121429_121431delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*609_*611delinsACC	ENSP00000508434.1:n.*609_*611delinsACC
ENST00000440875.6:c.-18_-16delinsACC	ENSP00000475553.3:n.-18_-16delinsACC
ENST00000627532.3:c.760_762delinsACC MANE Select	ENSP00000487174.1:p.Thr254=
ENST00000636026.2:c.760_762delinsACC	ENSP00000490776.1:p.Thr254=
ENST00000636179.1:n.729_731delinsACC
ENST00000636413.1:c.424_426delinsACC	ENSP00000490508.1:p.Thr142=
ENST00000636471.1:c.760_762delinsACC	ENSP00000490317.1:p.Thr254=
ENST00000636732.2:c.*477_*479delinsACC	ENSP00000490175.1:n.*477_*479delinsACC
ENST00000636820.1:n.860_862delinsACC
ENST00000637045.1:c.424_426delinsACC	ENSP00000490141.1:p.Thr142=
ENST00000637267.2:c.760_762delinsACC	ENSP00000490293.2:p.Thr254=
ENST00000637304.1:c.424_426delinsACC	ENSP00000490872.1:p.Thr142=
ENST00000638007.1:c.424_426delinsACC	ENSP00000490723.1:p.Thr142=
ENST00000638087.1:c.424_426delinsACC	ENSP00000490673.1:p.Thr142=
ENST00000638128.1:c.-18_-16delinsACC	ENSP00000490934.1:n.-18_-16delinsACC
ENST00000675069.1:c.-133-5113_-133-5111delinsACC	ENSP00000502467.1:n.-133-5113_-133-5111delinsACC
ENST00000303660.8:c.757_759delinsACC	ENSP00000302501.4:p.Thr253=
ENST00000392861.6:c.844_846delinsACC	ENSP00000376601.3:p.Thr282=
ENST00000409487.7:c.760_762delinsACC	ENSP00000386854.2:p.Thr254=
ENST00000419938.5:c.499_501delinsACC	ENSP00000394777.2:p.Thr167=
ENST00000427902.5:c.847_849delinsACC	ENSP00000395496.2:p.Thr283=
ENST00000440875.5:c.745_747delinsACC	ENSP00000475553.2:p.Thr249=
ENST00000539609.7:c.688_690delinsACC	ENSP00000443792.2:p.Thr230=
ENST00000558170.6:c.760_762delinsACC	ENSP00000454157.1:p.Thr254=
ENST00000627532.2:c.760_762delinsACC	ENSP00000487174.1:p.Thr254=
NM_001171653.1:c.688_690delinsACC	NP_001165124.1:p.Thr230=
NM_014795.3:c.760_762delinsACC	NP_055610.1:p.Thr254=
XM_006712881.2:c.760_762delinsACC	XP_006712944.1:p.Thr254=
XM_006712882.2:c.760_762delinsACC	XP_006712945.1:p.Thr254=
XM_011512231.1:c.751_753delinsACC	XP_011510533.1:p.Thr251=
XM_011512232.1:c.739_741delinsACC	XP_011510534.1:p.Thr247=
NM_014795.4:c.760_762delinsACC MANE Select	NP_055610.1:p.Thr254=
NM_001171653.2:c.688_690delinsACC	NP_001165124.1:p.Thr230=