Canonical Allele Identifier: CA2586970088

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398771del , CM000664.2:g.144398771del	GRCh38
NC_000002.11:g.145156338del , CM000664.1:g.145156338del	GRCh37
NC_000002.10:g.144872808del	NCBI36
NG_016431.1:g.126622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2266del	ENSP00000508434.1:n.*2266del
ENST00000440875.6:c.1640del	ENSP00000475553.3:p.Phe547SerfsTer11
ENST00000627532.3:c.2417del MANE Select	ENSP00000487174.1:p.Phe806SerfsTer11
ENST00000636026.2:c.2417del	ENSP00000490776.1:p.Phe806SerfsTer11
ENST00000636179.1:n.2386del
ENST00000636413.1:c.2081del	ENSP00000490508.1:p.Phe694SerfsTer11
ENST00000636471.1:c.2492del	ENSP00000490317.1:p.Phe831SerfsTer11
ENST00000636732.2:c.*2134del	ENSP00000490175.1:n.*2134del
ENST00000636820.1:n.2517del
ENST00000637045.1:c.2081del	ENSP00000490141.1:p.Phe694SerfsTer11
ENST00000637304.1:c.2081del	ENSP00000490872.1:p.Phe694SerfsTer11
ENST00000638007.1:c.2081del	ENSP00000490723.1:p.Phe694SerfsTer11
ENST00000638087.1:c.2081del	ENSP00000490673.1:p.Phe694SerfsTer11
ENST00000638128.1:c.1640del	ENSP00000490934.1:p.Phe547SerfsTer11
ENST00000675069.1:c.-53del	ENSP00000502467.1:n.-53del
ENST00000675145.1:n.2965del
ENST00000303660.8:c.2414del	ENSP00000302501.4:p.Phe805SerfsTer11
ENST00000409487.7:c.2417del	ENSP00000386854.2:p.Phe806SerfsTer11
ENST00000419938.5:c.655+2429del	ENSP00000394777.2:n.655+2429del
ENST00000440875.5:c.1167+767del	ENSP00000475553.2:n.1167+767del
ENST00000539609.7:c.2345del	ENSP00000443792.2:p.Phe782SerfsTer11
ENST00000558170.6:c.2417del	ENSP00000454157.1:p.Phe806SerfsTer11
ENST00000627532.2:c.2417del	ENSP00000487174.1:p.Phe806SerfsTer11
NM_001171653.1:c.2345del	NP_001165124.1:p.Phe782SerfsTer11
NM_014795.3:c.2417del	NP_055610.1:p.Phe806SerfsTer11
XM_006712881.2:c.2417del	XP_006712944.1:p.Phe806SerfsTer11
XM_006712882.2:c.2417del	XP_006712945.1:p.Phe806SerfsTer11
XM_011512231.1:c.2408del	XP_011510533.1:p.Phe803SerfsTer11
XM_011512232.1:c.2396del	XP_011510534.1:p.Phe799SerfsTer11
NM_014795.4:c.2417del MANE Select	NP_055610.1:p.Phe806SerfsTer11
NM_001171653.2:c.2345del	NP_001165124.1:p.Phe782SerfsTer11