Canonical Allele Identifier: CA658766350

Gene: ZEB2

Linked Data

• PubMed: PMID:28135719

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396488_144396489del , CM000664.2:g.144396488_144396489del	GRCh38
NC_000002.11:g.145154055_145154056del , CM000664.1:g.145154055_145154056del	GRCh37
NC_000002.10:g.144870525_144870526del	NCBI36
NG_016431.1:g.128903_128904del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2839_*2840del	ENSP00000508434.1:n.*2839_*2840del
ENST00000440875.6:c.2213_2214del	ENSP00000475553.3:p.Gly738AspfsTer5
ENST00000627532.3:c.2990_2991del MANE Select	ENSP00000487174.1:p.Gly997AspfsTer5
ENST00000636026.2:c.2990_2991del	ENSP00000490776.1:p.Gly997AspfsTer5
ENST00000636179.1:n.2959_2960del
ENST00000636413.1:c.2654_2655del	ENSP00000490508.1:p.Gly885AspfsTer5
ENST00000636471.1:c.3065_3066del	ENSP00000490317.1:p.Gly1022AspfsTer5
ENST00000636732.2:c.*2707_*2708del	ENSP00000490175.1:n.*2707_*2708del
ENST00000636820.1:n.3090_3091del
ENST00000637045.1:c.2654_2655del	ENSP00000490141.1:p.Gly885AspfsTer5
ENST00000637304.1:c.2654_2655del	ENSP00000490872.1:p.Gly885AspfsTer5
ENST00000638007.1:c.2654_2655del	ENSP00000490723.1:p.Gly885AspfsTer5
ENST00000638087.1:c.2654_2655del	ENSP00000490673.1:p.Gly885AspfsTer5
ENST00000638128.1:c.2213_2214del	ENSP00000490934.1:p.Gly738AspfsTer5
ENST00000639389.1:c.74_75del	ENSP00000492572.1:p.Gly25AspfsTer5
ENST00000647488.1:c.122_123del	ENSP00000494820.1:p.Gly41AspfsTer5
ENST00000675069.1:c.521_522del	ENSP00000502467.1:p.Gly174AspfsTer5
ENST00000303660.8:c.2987_2988del	ENSP00000302501.4:p.Gly996AspfsTer5
ENST00000409487.7:c.2990_2991del	ENSP00000386854.2:p.Gly997AspfsTer5
ENST00000419938.5:c.655+4710_655+4711del	ENSP00000394777.2:n.655+4710_655+4711del
ENST00000539609.7:c.2918_2919del	ENSP00000443792.2:p.Gly973AspfsTer5
ENST00000558170.6:c.2990_2991del	ENSP00000454157.1:p.Gly997AspfsTer5
ENST00000627532.2:c.2990_2991del	ENSP00000487174.1:p.Gly997AspfsTer5
NM_001171653.1:c.2918_2919del	NP_001165124.1:p.Gly973AspfsTer5
NM_014795.3:c.2990_2991del	NP_055610.1:p.Gly997AspfsTer5
XM_006712881.2:c.2990_2991del	XP_006712944.1:p.Gly997AspfsTer5
XM_006712882.2:c.2990_2991del	XP_006712945.1:p.Gly997AspfsTer5
XM_011512231.1:c.2981_2982del	XP_011510533.1:p.Gly994AspfsTer5
XM_011512232.1:c.2969_2970del	XP_011510534.1:p.Gly990AspfsTer5
NM_014795.4:c.2990_2991del MANE Select	NP_055610.1:p.Gly997AspfsTer5
NM_001171653.2:c.2918_2919del	NP_001165124.1:p.Gly973AspfsTer5