Canonical Allele Identifier: CA2586969978

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389716del , CM000664.2:g.144389716del	GRCh38
NC_000002.11:g.145147283del , CM000664.1:g.145147283del	GRCh37
NC_000002.10:g.144863753del	NCBI36
NG_016431.1:g.135678del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3231del	ENSP00000508434.1:n.*3231del
ENST00000440875.6:c.2605del	ENSP00000475553.3:p.Glu869ArgfsTer?
ENST00000627532.3:c.3382del MANE Select	ENSP00000487174.1:p.Glu1128ArgfsTer?
ENST00000636026.2:c.3270del	ENSP00000490776.1:p.Arg1091GlufsTer?
ENST00000636179.1:n.3351del
ENST00000636413.1:c.3046del	ENSP00000490508.1:p.Glu1016ArgfsTer?
ENST00000636471.1:c.3457del	ENSP00000490317.1:p.Glu1153ArgfsTer?
ENST00000636732.2:c.*3099del	ENSP00000490175.1:n.*3099del
ENST00000636820.1:n.3482del
ENST00000637045.1:c.3046del	ENSP00000490141.1:p.Glu1016ArgfsTer?
ENST00000637304.1:c.3046del	ENSP00000490872.1:p.Glu1016ArgfsTer?
ENST00000638007.1:c.3046del	ENSP00000490723.1:p.Glu1016ArgfsTer?
ENST00000638087.1:c.3046del	ENSP00000490673.1:p.Glu1016ArgfsTer?
ENST00000638128.1:c.2605del	ENSP00000490934.1:p.Glu869ArgfsTer?
ENST00000639389.1:c.151+6698del	ENSP00000492572.1:n.151+6698del
ENST00000647488.1:c.602del	ENSP00000494820.1:n.602del
ENST00000675069.1:c.913del	ENSP00000502467.1:p.Glu305ArgfsTer?
ENST00000303660.8:c.3379del	ENSP00000302501.4:p.Glu1127ArgfsTer?
ENST00000409487.7:c.3382del	ENSP00000386854.2:p.Glu1128ArgfsTer?
ENST00000419938.5:c.656-832del	ENSP00000394777.2:n.656-832del
ENST00000539609.7:c.3310del	ENSP00000443792.2:p.Glu1104ArgfsTer?
ENST00000558170.6:c.3382del	ENSP00000454157.1:p.Glu1128ArgfsTer?
ENST00000627532.2:c.3382del	ENSP00000487174.1:p.Glu1128ArgfsTer?
NM_001171653.1:c.3310del	NP_001165124.1:p.Glu1104ArgfsTer?
NM_014795.3:c.3382del	NP_055610.1:p.Glu1128ArgfsTer?
XM_006712881.2:c.3382del	XP_006712944.1:p.Glu1128ArgfsTer?
XM_006712882.2:c.3382del	XP_006712945.1:p.Glu1128ArgfsTer?
XM_011512231.1:c.3373del	XP_011510533.1:p.Glu1125ArgfsTer?
XM_011512232.1:c.3361del	XP_011510534.1:p.Glu1121ArgfsTer?
NM_014795.4:c.3382del MANE Select	NP_055610.1:p.Glu1128ArgfsTer?
NM_001171653.2:c.3310del	NP_001165124.1:p.Glu1104ArgfsTer?