Canonical Allele Identifier: CA2499214971
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1071230
ClinVar RCV Id: RCV001383647
dbSNP Id: rs2149876500

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398598del , CM000664.2:g.144398598del GRCh38
NC_000002.11:g.145156165del , CM000664.1:g.145156165del GRCh37
NC_000002.10:g.144872635del NCBI36
NG_016431.1:g.126797del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2441del ENSP00000508434.1:n.*2441del
ENST00000440875.6:c.1815del ENSP00000475553.3:p.Phe605LeufsTer23
ENST00000627532.3:c.2592del MANE Select ENSP00000487174.1:p.Phe864LeufsTer23
ENST00000636026.2:c.2592del ENSP00000490776.1:p.Phe864LeufsTer23
ENST00000636179.1:n.2561del
ENST00000636413.1:c.2256del ENSP00000490508.1:p.Phe752LeufsTer23
ENST00000636471.1:c.2667del ENSP00000490317.1:p.Phe889LeufsTer23
ENST00000636732.2:c.*2309del ENSP00000490175.1:n.*2309del
ENST00000636820.1:n.2692del
ENST00000637045.1:c.2256del ENSP00000490141.1:p.Phe752LeufsTer23
ENST00000637304.1:c.2256del ENSP00000490872.1:p.Phe752LeufsTer23
ENST00000638007.1:c.2256del ENSP00000490723.1:p.Phe752LeufsTer23
ENST00000638087.1:c.2256del ENSP00000490673.1:p.Phe752LeufsTer23
ENST00000638128.1:c.1815del ENSP00000490934.1:p.Phe605LeufsTer23
ENST00000675069.1:c.123del ENSP00000502467.1:p.Phe41LeufsTer23
ENST00000303660.8:c.2589del ENSP00000302501.4:p.Phe863LeufsTer23
ENST00000409487.7:c.2592del ENSP00000386854.2:p.Phe864LeufsTer23
ENST00000419938.5:c.655+2604del ENSP00000394777.2:n.655+2604del
ENST00000440875.5:c.1168-667del ENSP00000475553.2:n.1168-667del
ENST00000539609.7:c.2520del ENSP00000443792.2:p.Phe840LeufsTer23
ENST00000558170.6:c.2592del ENSP00000454157.1:p.Phe864LeufsTer23
ENST00000627532.2:c.2592del ENSP00000487174.1:p.Phe864LeufsTer23
NM_001171653.1:c.2520del NP_001165124.1:p.Phe840LeufsTer23
NM_014795.3:c.2592del NP_055610.1:p.Phe864LeufsTer23
XM_006712881.2:c.2592del XP_006712944.1:p.Phe864LeufsTer23
XM_006712882.2:c.2592del XP_006712945.1:p.Phe864LeufsTer23
XM_011512231.1:c.2583del XP_011510533.1:p.Phe861LeufsTer23
XM_011512232.1:c.2571del XP_011510534.1:p.Phe857LeufsTer23
NM_014795.4:c.2592del MANE Select NP_055610.1:p.Phe864LeufsTer23
NM_001171653.2:c.2520del NP_001165124.1:p.Phe840LeufsTer23