Canonical Allele Identifier: CA2586970077

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398510_144398515del , CM000664.2:g.144398510_144398515del	GRCh38
NC_000002.11:g.145156077_145156082del , CM000664.1:g.145156077_145156082del	GRCh37
NC_000002.10:g.144872547_144872552del	NCBI36
NG_016431.1:g.126878_126883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2522_*2527del	ENSP00000508434.1:n.*2522_*2527del
ENST00000440875.6:c.1896_1901del	ENSP00000475553.3:p.Lys633_Pro634del
ENST00000627532.3:c.2673_2678del MANE Select	ENSP00000487174.1:p.Lys892_Pro893del
ENST00000636026.2:c.2673_2678del	ENSP00000490776.1:p.Lys892_Pro893del
ENST00000636179.1:n.2642_2647del
ENST00000636413.1:c.2337_2342del	ENSP00000490508.1:p.Lys780_Pro781del
ENST00000636471.1:c.2748_2753del	ENSP00000490317.1:p.Lys917_Pro918del
ENST00000636732.2:c.*2390_*2395del	ENSP00000490175.1:n.*2390_*2395del
ENST00000636820.1:n.2773_2778del
ENST00000637045.1:c.2337_2342del	ENSP00000490141.1:p.Lys780_Pro781del
ENST00000637304.1:c.2337_2342del	ENSP00000490872.1:p.Lys780_Pro781del
ENST00000638007.1:c.2337_2342del	ENSP00000490723.1:p.Lys780_Pro781del
ENST00000638087.1:c.2337_2342del	ENSP00000490673.1:p.Lys780_Pro781del
ENST00000638128.1:c.1896_1901del	ENSP00000490934.1:p.Lys633_Pro634del
ENST00000675069.1:c.204_209del	ENSP00000502467.1:p.Lys69_Pro70del
ENST00000303660.8:c.2670_2675del	ENSP00000302501.4:p.Lys891_Pro892del
ENST00000409487.7:c.2673_2678del	ENSP00000386854.2:p.Lys892_Pro893del
ENST00000419938.5:c.655+2685_655+2690del	ENSP00000394777.2:n.655+2685_655+2690del
ENST00000440875.5:c.1168-586_1168-581del	ENSP00000475553.2:n.1168-586_1168-581del
ENST00000539609.7:c.2601_2606del	ENSP00000443792.2:p.Lys868_Pro869del
ENST00000558170.6:c.2673_2678del	ENSP00000454157.1:p.Lys892_Pro893del
ENST00000627532.2:c.2673_2678del	ENSP00000487174.1:p.Lys892_Pro893del
NM_001171653.1:c.2601_2606del	NP_001165124.1:p.Lys868_Pro869del
NM_014795.3:c.2673_2678del	NP_055610.1:p.Lys892_Pro893del
XM_006712881.2:c.2673_2678del	XP_006712944.1:p.Lys892_Pro893del
XM_006712882.2:c.2673_2678del	XP_006712945.1:p.Lys892_Pro893del
XM_011512231.1:c.2664_2669del	XP_011510533.1:p.Lys889_Pro890del
XM_011512232.1:c.2652_2657del	XP_011510534.1:p.Lys885_Pro886del
NM_014795.4:c.2673_2678del MANE Select	NP_055610.1:p.Lys892_Pro893del
NM_001171653.2:c.2601_2606del	NP_001165124.1:p.Lys868_Pro869del