Canonical Allele Identifier: CA2586970092
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398869_144398870del , CM000664.2:g.144398869_144398870del GRCh38
NC_000002.11:g.145156436_145156437del , CM000664.1:g.145156436_145156437del GRCh37
NC_000002.10:g.144872906_144872907del NCBI36
NG_016431.1:g.126522_126523del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2166_*2167del ENSP00000508434.1:n.*2166_*2167del
ENST00000440875.6:c.1540_1541del ENSP00000475553.3:p.Glu514LysfsTer8
ENST00000627532.3:c.2317_2318del MANE Select ENSP00000487174.1:p.Glu773LysfsTer8
ENST00000636026.2:c.2317_2318del ENSP00000490776.1:p.Glu773LysfsTer8
ENST00000636179.1:n.2286_2287del
ENST00000636413.1:c.1981_1982del ENSP00000490508.1:p.Glu661LysfsTer8
ENST00000636471.1:c.2392_2393del ENSP00000490317.1:p.Glu798LysfsTer8
ENST00000636732.2:c.*2034_*2035del ENSP00000490175.1:n.*2034_*2035del
ENST00000636820.1:n.2417_2418del
ENST00000637045.1:c.1981_1982del ENSP00000490141.1:p.Glu661LysfsTer8
ENST00000637304.1:c.1981_1982del ENSP00000490872.1:p.Glu661LysfsTer8
ENST00000638007.1:c.1981_1982del ENSP00000490723.1:p.Glu661LysfsTer8
ENST00000638087.1:c.1981_1982del ENSP00000490673.1:p.Glu661LysfsTer8
ENST00000638128.1:c.1540_1541del ENSP00000490934.1:p.Glu514LysfsTer8
ENST00000675069.1:c.-133-20_-133-19del ENSP00000502467.1:n.-133-20_-133-19del
ENST00000675145.1:n.2865_2866del
ENST00000303660.8:c.2314_2315del ENSP00000302501.4:p.Glu772LysfsTer8
ENST00000409487.7:c.2317_2318del ENSP00000386854.2:p.Glu773LysfsTer8
ENST00000419938.5:c.655+2329_655+2330del ENSP00000394777.2:n.655+2329_655+2330del
ENST00000440875.5:c.1167+667_1167+668del ENSP00000475553.2:n.1167+667_1167+668del
ENST00000539609.7:c.2245_2246del ENSP00000443792.2:p.Glu749LysfsTer8
ENST00000558170.6:c.2317_2318del ENSP00000454157.1:p.Glu773LysfsTer8
ENST00000627532.2:c.2317_2318del ENSP00000487174.1:p.Glu773LysfsTer8
NM_001171653.1:c.2245_2246del NP_001165124.1:p.Glu749LysfsTer8
NM_014795.3:c.2317_2318del NP_055610.1:p.Glu773LysfsTer8
XM_006712881.2:c.2317_2318del XP_006712944.1:p.Glu773LysfsTer8
XM_006712882.2:c.2317_2318del XP_006712945.1:p.Glu773LysfsTer8
XM_011512231.1:c.2308_2309del XP_011510533.1:p.Glu770LysfsTer8
XM_011512232.1:c.2296_2297del XP_011510534.1:p.Glu766LysfsTer8
NM_014795.4:c.2317_2318del MANE Select NP_055610.1:p.Glu773LysfsTer8
NM_001171653.2:c.2245_2246del NP_001165124.1:p.Glu749LysfsTer8