Canonical Allele Identifier: CA2586970089

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398815del , CM000664.2:g.144398815del	GRCh38
NC_000002.11:g.145156382del , CM000664.1:g.145156382del	GRCh37
NC_000002.10:g.144872852del	NCBI36
NG_016431.1:g.126577del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2221del	ENSP00000508434.1:n.*2221del
ENST00000440875.6:c.1595del	ENSP00000475553.3:p.Thr532AsnfsTer26
ENST00000627532.3:c.2372del MANE Select	ENSP00000487174.1:p.Thr791AsnfsTer26
ENST00000636026.2:c.2372del	ENSP00000490776.1:p.Thr791AsnfsTer26
ENST00000636179.1:n.2341del
ENST00000636413.1:c.2036del	ENSP00000490508.1:p.Thr679AsnfsTer26
ENST00000636471.1:c.2447del	ENSP00000490317.1:p.Thr816AsnfsTer26
ENST00000636732.2:c.*2089del	ENSP00000490175.1:n.*2089del
ENST00000636820.1:n.2472del
ENST00000637045.1:c.2036del	ENSP00000490141.1:p.Thr679AsnfsTer26
ENST00000637304.1:c.2036del	ENSP00000490872.1:p.Thr679AsnfsTer26
ENST00000638007.1:c.2036del	ENSP00000490723.1:p.Thr679AsnfsTer26
ENST00000638087.1:c.2036del	ENSP00000490673.1:p.Thr679AsnfsTer26
ENST00000638128.1:c.1595del	ENSP00000490934.1:p.Thr532AsnfsTer26
ENST00000675069.1:c.-98del	ENSP00000502467.1:n.-98del
ENST00000675145.1:n.2920del
ENST00000303660.8:c.2369del	ENSP00000302501.4:p.Thr790AsnfsTer26
ENST00000409487.7:c.2372del	ENSP00000386854.2:p.Thr791AsnfsTer26
ENST00000419938.5:c.655+2384del	ENSP00000394777.2:n.655+2384del
ENST00000440875.5:c.1167+722del	ENSP00000475553.2:n.1167+722del
ENST00000539609.7:c.2300del	ENSP00000443792.2:p.Thr767AsnfsTer26
ENST00000558170.6:c.2372del	ENSP00000454157.1:p.Thr791AsnfsTer26
ENST00000627532.2:c.2372del	ENSP00000487174.1:p.Thr791AsnfsTer26
NM_001171653.1:c.2300del	NP_001165124.1:p.Thr767AsnfsTer26
NM_014795.3:c.2372del	NP_055610.1:p.Thr791AsnfsTer26
XM_006712881.2:c.2372del	XP_006712944.1:p.Thr791AsnfsTer26
XM_006712882.2:c.2372del	XP_006712945.1:p.Thr791AsnfsTer26
XM_011512231.1:c.2363del	XP_011510533.1:p.Thr788AsnfsTer26
XM_011512232.1:c.2351del	XP_011510534.1:p.Thr784AsnfsTer26
NM_014795.4:c.2372del MANE Select	NP_055610.1:p.Thr791AsnfsTer26
NM_001171653.2:c.2300del	NP_001165124.1:p.Thr767AsnfsTer26