Canonical Allele Identifier: CA2517145042

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398476_144398477insCA , CM000664.2:g.144398476_144398477insCA	GRCh38
NC_000002.11:g.145156043_145156044insCA , CM000664.1:g.145156043_145156044insCA	GRCh37
NC_000002.10:g.144872513_144872514insCA	NCBI36
NG_016431.1:g.126916_126917insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2560_*2561insGT	ENSP00000508434.1:n.*2560_*2561insGT
ENST00000440875.6:c.1934_1935insGT	ENSP00000475553.3:p.Phe645LeufsTer27
ENST00000627532.3:c.2711_2712insGT MANE Select	ENSP00000487174.1:p.Phe904LeufsTer27
ENST00000636026.2:c.2711_2712insGT	ENSP00000490776.1:p.Phe904LeufsTer27
ENST00000636179.1:n.2680_2681insGT
ENST00000636413.1:c.2375_2376insGT	ENSP00000490508.1:p.Phe792LeufsTer27
ENST00000636471.1:c.2786_2787insGT	ENSP00000490317.1:p.Phe929LeufsTer27
ENST00000636732.2:c.*2428_*2429insGT	ENSP00000490175.1:n.*2428_*2429insGT
ENST00000636820.1:n.2811_2812insGT
ENST00000637045.1:c.2375_2376insGT	ENSP00000490141.1:p.Phe792LeufsTer27
ENST00000637304.1:c.2375_2376insGT	ENSP00000490872.1:p.Phe792LeufsTer27
ENST00000638007.1:c.2375_2376insGT	ENSP00000490723.1:p.Phe792LeufsTer27
ENST00000638087.1:c.2375_2376insGT	ENSP00000490673.1:p.Phe792LeufsTer27
ENST00000638128.1:c.1934_1935insGT	ENSP00000490934.1:p.Phe645LeufsTer27
ENST00000675069.1:c.242_243insGT	ENSP00000502467.1:p.Phe81LeufsTer27
ENST00000303660.8:c.2708_2709insGT	ENSP00000302501.4:p.Phe903LeufsTer27
ENST00000409487.7:c.2711_2712insGT	ENSP00000386854.2:p.Phe904LeufsTer27
ENST00000419938.5:c.655+2723_655+2724insGT	ENSP00000394777.2:n.655+2723_655+2724insGT
ENST00000440875.5:c.1168-548_1168-547insGT	ENSP00000475553.2:n.1168-548_1168-547insGT
ENST00000539609.7:c.2639_2640insGT	ENSP00000443792.2:p.Phe880LeufsTer27
ENST00000558170.6:c.2711_2712insGT	ENSP00000454157.1:p.Phe904LeufsTer27
ENST00000627532.2:c.2711_2712insGT	ENSP00000487174.1:p.Phe904LeufsTer27
NM_001171653.1:c.2639_2640insGT	NP_001165124.1:p.Phe880LeufsTer27
NM_014795.3:c.2711_2712insGT	NP_055610.1:p.Phe904LeufsTer27
XM_006712881.2:c.2711_2712insGT	XP_006712944.1:p.Phe904LeufsTer27
XM_006712882.2:c.2711_2712insGT	XP_006712945.1:p.Phe904LeufsTer27
XM_011512231.1:c.2702_2703insGT	XP_011510533.1:p.Phe901LeufsTer27
XM_011512232.1:c.2690_2691insGT	XP_011510534.1:p.Phe897LeufsTer27
NM_014795.4:c.2711_2712insGT MANE Select	NP_055610.1:p.Phe904LeufsTer27
NM_001171653.2:c.2639_2640insGT	NP_001165124.1:p.Phe880LeufsTer27