Canonical Allele Identifier: CA2586970080

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398512_144398531dup , CM000664.2:g.144398512_144398531dup	GRCh38
NC_000002.11:g.145156079_145156098dup , CM000664.1:g.145156079_145156098dup	GRCh37
NC_000002.10:g.144872549_144872568dup	NCBI36
NG_016431.1:g.126862_126881dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2506_*2525dup	ENSP00000508434.1:n.*2506_*2525dup
ENST00000440875.6:c.1880_1899dup	ENSP00000475553.3:p.Pro634Ter
ENST00000627532.3:c.2657_2676dup MANE Select	ENSP00000487174.1:p.Pro893Ter
ENST00000636026.2:c.2657_2676dup	ENSP00000490776.1:p.Pro893Ter
ENST00000636179.1:n.2626_2645dup
ENST00000636413.1:c.2321_2340dup	ENSP00000490508.1:p.Pro781Ter
ENST00000636471.1:c.2732_2751dup	ENSP00000490317.1:p.Pro918Ter
ENST00000636732.2:c.*2374_*2393dup	ENSP00000490175.1:n.*2374_*2393dup
ENST00000636820.1:n.2757_2776dup
ENST00000637045.1:c.2321_2340dup	ENSP00000490141.1:p.Pro781Ter
ENST00000637304.1:c.2321_2340dup	ENSP00000490872.1:p.Pro781Ter
ENST00000638007.1:c.2321_2340dup	ENSP00000490723.1:p.Pro781Ter
ENST00000638087.1:c.2321_2340dup	ENSP00000490673.1:p.Pro781Ter
ENST00000638128.1:c.1880_1899dup	ENSP00000490934.1:p.Pro634Ter
ENST00000675069.1:c.188_207dup	ENSP00000502467.1:p.Pro70Ter
ENST00000303660.8:c.2654_2673dup	ENSP00000302501.4:p.Pro892Ter
ENST00000409487.7:c.2657_2676dup	ENSP00000386854.2:p.Pro893Ter
ENST00000419938.5:c.655+2669_655+2688dup	ENSP00000394777.2:n.655+2669_655+2688dup
ENST00000440875.5:c.1168-602_1168-583dup	ENSP00000475553.2:n.1168-602_1168-583dup
ENST00000539609.7:c.2585_2604dup	ENSP00000443792.2:p.Pro869Ter
ENST00000558170.6:c.2657_2676dup	ENSP00000454157.1:p.Pro893Ter
ENST00000627532.2:c.2657_2676dup	ENSP00000487174.1:p.Pro893Ter
NM_001171653.1:c.2585_2604dup	NP_001165124.1:p.Pro869Ter
NM_014795.3:c.2657_2676dup	NP_055610.1:p.Pro893Ter
XM_006712881.2:c.2657_2676dup	XP_006712944.1:p.Pro893Ter
XM_006712882.2:c.2657_2676dup	XP_006712945.1:p.Pro893Ter
XM_011512231.1:c.2648_2667dup	XP_011510533.1:p.Pro890Ter
XM_011512232.1:c.2636_2655dup	XP_011510534.1:p.Pro886Ter
NM_014795.4:c.2657_2676dup MANE Select	NP_055610.1:p.Pro893Ter
NM_001171653.2:c.2585_2604dup	NP_001165124.1:p.Pro869Ter