Canonical Allele Identifier: CA2586970111

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399365del , CM000664.2:g.144399365del	GRCh38
NC_000002.11:g.145156932del , CM000664.1:g.145156932del	GRCh37
NC_000002.10:g.144873402del	NCBI36
NG_016431.1:g.126027del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1671del	ENSP00000508434.1:n.*1671del
ENST00000440875.6:c.1045del	ENSP00000475553.3:p.Glu349LysfsTer13
ENST00000627532.3:c.1822del MANE Select	ENSP00000487174.1:p.Glu608LysfsTer13
ENST00000636026.2:c.1822del	ENSP00000490776.1:p.Glu608LysfsTer13
ENST00000636179.1:n.1791del
ENST00000636413.1:c.1486del	ENSP00000490508.1:p.Glu496LysfsTer13
ENST00000636471.1:c.1897del	ENSP00000490317.1:p.Glu633LysfsTer13
ENST00000636732.2:c.*1539del	ENSP00000490175.1:n.*1539del
ENST00000636820.1:n.1922del
ENST00000637045.1:c.1486del	ENSP00000490141.1:p.Glu496LysfsTer13
ENST00000637267.2:c.1822del	ENSP00000490293.2:p.Glu608LysfsTer?
ENST00000637304.1:c.1486del	ENSP00000490872.1:p.Glu496LysfsTer13
ENST00000638007.1:c.1486del	ENSP00000490723.1:p.Glu496LysfsTer13
ENST00000638087.1:c.1486del	ENSP00000490673.1:p.Glu496LysfsTer13
ENST00000638128.1:c.1045del	ENSP00000490934.1:p.Glu349LysfsTer13
ENST00000675069.1:c.-133-515del	ENSP00000502467.1:n.-133-515del
ENST00000675145.1:n.2370del
ENST00000303660.8:c.1819del	ENSP00000302501.4:p.Glu607LysfsTer13
ENST00000409487.7:c.1822del	ENSP00000386854.2:p.Glu608LysfsTer13
ENST00000419938.5:c.655+1834del	ENSP00000394777.2:n.655+1834del
ENST00000427902.5:c.1909del	ENSP00000395496.2:p.Glu637LysfsTer13
ENST00000440875.5:c.1167+172del	ENSP00000475553.2:n.1167+172del
ENST00000539609.7:c.1750del	ENSP00000443792.2:p.Glu584LysfsTer13
ENST00000558170.6:c.1822del	ENSP00000454157.1:p.Glu608LysfsTer13
ENST00000627532.2:c.1822del	ENSP00000487174.1:p.Glu608LysfsTer13
NM_001171653.1:c.1750del	NP_001165124.1:p.Glu584LysfsTer13
NM_014795.3:c.1822del	NP_055610.1:p.Glu608LysfsTer13
XM_006712881.2:c.1822del	XP_006712944.1:p.Glu608LysfsTer13
XM_006712882.2:c.1822del	XP_006712945.1:p.Glu608LysfsTer13
XM_011512231.1:c.1813del	XP_011510533.1:p.Glu605LysfsTer13
XM_011512232.1:c.1801del	XP_011510534.1:p.Glu601LysfsTer13
NM_014795.4:c.1822del MANE Select	NP_055610.1:p.Glu608LysfsTer13
NM_001171653.2:c.1750del	NP_001165124.1:p.Glu584LysfsTer13