Canonical Allele Identifier: CA2586970109
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399328_144399329del , CM000664.2:g.144399328_144399329del GRCh38
NC_000002.11:g.145156895_145156896del , CM000664.1:g.145156895_145156896del GRCh37
NC_000002.10:g.144873365_144873366del NCBI36
NG_016431.1:g.126064_126065del

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1708_*1709del ENSP00000508434.1:n.*1708_*1709del
ENST00000440875.6:c.1082_1083del ENSP00000475553.3:p.Ile361SerfsTer10
ENST00000627532.3:c.1859_1860del MANE Select ENSP00000487174.1:p.Ile620SerfsTer10
ENST00000636026.2:c.1859_1860del ENSP00000490776.1:p.Ile620SerfsTer10
ENST00000636179.1:n.1828_1829del
ENST00000636413.1:c.1523_1524del ENSP00000490508.1:p.Ile508SerfsTer10
ENST00000636471.1:c.1934_1935del ENSP00000490317.1:p.Ile645SerfsTer10
ENST00000636732.2:c.*1576_*1577del ENSP00000490175.1:n.*1576_*1577del
ENST00000636820.1:n.1959_1960del
ENST00000637045.1:c.1523_1524del ENSP00000490141.1:p.Ile508SerfsTer10
ENST00000637304.1:c.1523_1524del ENSP00000490872.1:p.Ile508SerfsTer10
ENST00000638007.1:c.1523_1524del ENSP00000490723.1:p.Ile508SerfsTer10
ENST00000638087.1:c.1523_1524del ENSP00000490673.1:p.Ile508SerfsTer10
ENST00000638128.1:c.1082_1083del ENSP00000490934.1:p.Ile361SerfsTer10
ENST00000675069.1:c.-133-478_-133-477del ENSP00000502467.1:n.-133-478_-133-477del
ENST00000675145.1:n.2407_2408del
ENST00000303660.8:c.1856_1857del ENSP00000302501.4:p.Ile619SerfsTer10
ENST00000409487.7:c.1859_1860del ENSP00000386854.2:p.Ile620SerfsTer10
ENST00000419938.5:c.655+1871_655+1872del ENSP00000394777.2:n.655+1871_655+1872del
ENST00000427902.5:c.1946_1947del ENSP00000395496.2:p.Ile649SerfsTer10
ENST00000440875.5:c.1167+209_1167+210del ENSP00000475553.2:n.1167+209_1167+210del
ENST00000539609.7:c.1787_1788del ENSP00000443792.2:p.Ile596SerfsTer10
ENST00000558170.6:c.1859_1860del ENSP00000454157.1:p.Ile620SerfsTer10
ENST00000627532.2:c.1859_1860del ENSP00000487174.1:p.Ile620SerfsTer10
NM_001171653.1:c.1787_1788del NP_001165124.1:p.Ile596SerfsTer10
NM_014795.3:c.1859_1860del NP_055610.1:p.Ile620SerfsTer10
XM_006712881.2:c.1859_1860del XP_006712944.1:p.Ile620SerfsTer10
XM_006712882.2:c.1859_1860del XP_006712945.1:p.Ile620SerfsTer10
XM_011512231.1:c.1850_1851del XP_011510533.1:p.Ile617SerfsTer10
XM_011512232.1:c.1838_1839del XP_011510534.1:p.Ile613SerfsTer10
NM_014795.4:c.1859_1860del MANE Select NP_055610.1:p.Ile620SerfsTer10
NM_001171653.2:c.1787_1788del NP_001165124.1:p.Ile596SerfsTer10