Canonical Allele Identifier: CA2586970073

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398448del , CM000664.2:g.144398448del	GRCh38
NC_000002.11:g.145156015del , CM000664.1:g.145156015del	GRCh37
NC_000002.10:g.144872485del	NCBI36
NG_016431.1:g.126945del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2589del	ENSP00000508434.1:n.*2589del
ENST00000440875.6:c.1963del	ENSP00000475553.3:p.Gln655ArgfsTer16
ENST00000627532.3:c.2740del MANE Select	ENSP00000487174.1:p.Gln914ArgfsTer16
ENST00000636026.2:c.2740del	ENSP00000490776.1:p.Gln914ArgfsTer16
ENST00000636179.1:n.2709del
ENST00000636413.1:c.2404del	ENSP00000490508.1:p.Gln802ArgfsTer16
ENST00000636471.1:c.2815del	ENSP00000490317.1:p.Gln939ArgfsTer16
ENST00000636732.2:c.*2457del	ENSP00000490175.1:n.*2457del
ENST00000636820.1:n.2840del
ENST00000637045.1:c.2404del	ENSP00000490141.1:p.Gln802ArgfsTer16
ENST00000637304.1:c.2404del	ENSP00000490872.1:p.Gln802ArgfsTer16
ENST00000638007.1:c.2404del	ENSP00000490723.1:p.Gln802ArgfsTer16
ENST00000638087.1:c.2404del	ENSP00000490673.1:p.Gln802ArgfsTer16
ENST00000638128.1:c.1963del	ENSP00000490934.1:p.Gln655ArgfsTer16
ENST00000675069.1:c.271del	ENSP00000502467.1:p.Gln91ArgfsTer16
ENST00000303660.8:c.2737del	ENSP00000302501.4:p.Gln913ArgfsTer16
ENST00000409487.7:c.2740del	ENSP00000386854.2:p.Gln914ArgfsTer16
ENST00000419938.5:c.655+2752del	ENSP00000394777.2:n.655+2752del
ENST00000440875.5:c.1168-519del	ENSP00000475553.2:n.1168-519del
ENST00000539609.7:c.2668del	ENSP00000443792.2:p.Gln890ArgfsTer16
ENST00000558170.6:c.2740del	ENSP00000454157.1:p.Gln914ArgfsTer16
ENST00000627532.2:c.2740del	ENSP00000487174.1:p.Gln914ArgfsTer16
NM_001171653.1:c.2668del	NP_001165124.1:p.Gln890ArgfsTer16
NM_014795.3:c.2740del	NP_055610.1:p.Gln914ArgfsTer16
XM_006712881.2:c.2740del	XP_006712944.1:p.Gln914ArgfsTer16
XM_006712882.2:c.2740del	XP_006712945.1:p.Gln914ArgfsTer16
XM_011512231.1:c.2731del	XP_011510533.1:p.Gln911ArgfsTer16
XM_011512232.1:c.2719del	XP_011510534.1:p.Gln907ArgfsTer16
NM_014795.4:c.2740del MANE Select	NP_055610.1:p.Gln914ArgfsTer16
NM_001171653.2:c.2668del	NP_001165124.1:p.Gln890ArgfsTer16