Canonical Allele Identifier: CA2580063839
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1703405

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398469del , CM000664.2:g.144398469del GRCh38
NC_000002.11:g.145156036del , CM000664.1:g.145156036del GRCh37
NC_000002.10:g.144872506del NCBI36
NG_016431.1:g.126923del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2567del ENSP00000508434.1:n.*2567del
ENST00000440875.6:c.1941del ENSP00000475553.3:p.Ala648LeufsTer23
ENST00000627532.3:c.2718del MANE Select ENSP00000487174.1:p.Ala907LeufsTer23
ENST00000636026.2:c.2718del ENSP00000490776.1:p.Ala907LeufsTer23
ENST00000636179.1:n.2687del
ENST00000636413.1:c.2382del ENSP00000490508.1:p.Ala795LeufsTer23
ENST00000636471.1:c.2793del ENSP00000490317.1:p.Ala932LeufsTer23
ENST00000636732.2:c.*2435del ENSP00000490175.1:n.*2435del
ENST00000636820.1:n.2818del
ENST00000637045.1:c.2382del ENSP00000490141.1:p.Ala795LeufsTer23
ENST00000637304.1:c.2382del ENSP00000490872.1:p.Ala795LeufsTer23
ENST00000638007.1:c.2382del ENSP00000490723.1:p.Ala795LeufsTer23
ENST00000638087.1:c.2382del ENSP00000490673.1:p.Ala795LeufsTer23
ENST00000638128.1:c.1941del ENSP00000490934.1:p.Ala648LeufsTer23
ENST00000675069.1:c.249del ENSP00000502467.1:p.Ala84LeufsTer23
ENST00000303660.8:c.2715del ENSP00000302501.4:p.Ala906LeufsTer23
ENST00000409487.7:c.2718del ENSP00000386854.2:p.Ala907LeufsTer23
ENST00000419938.5:c.655+2730del ENSP00000394777.2:n.655+2730del
ENST00000440875.5:c.1168-541del ENSP00000475553.2:n.1168-541del
ENST00000539609.7:c.2646del ENSP00000443792.2:p.Ala883LeufsTer23
ENST00000558170.6:c.2718del ENSP00000454157.1:p.Ala907LeufsTer23
ENST00000627532.2:c.2718del ENSP00000487174.1:p.Ala907LeufsTer23
NM_001171653.1:c.2646del NP_001165124.1:p.Ala883LeufsTer23
NM_014795.3:c.2718del NP_055610.1:p.Ala907LeufsTer23
XM_006712881.2:c.2718del XP_006712944.1:p.Ala907LeufsTer23
XM_006712882.2:c.2718del XP_006712945.1:p.Ala907LeufsTer23
XM_011512231.1:c.2709del XP_011510533.1:p.Ala904LeufsTer23
XM_011512232.1:c.2697del XP_011510534.1:p.Ala900LeufsTer23
NM_014795.4:c.2718del MANE Select NP_055610.1:p.Ala907LeufsTer23
NM_001171653.2:c.2646del NP_001165124.1:p.Ala883LeufsTer23