Canonical Allele Identifier: CA348710159
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399389C>T , CM000664.2:g.144399389C>T GRCh38
NC_000002.11:g.145156956C>T , CM000664.1:g.145156956C>T GRCh37
NC_000002.10:g.144873426C>T NCBI36
NG_016431.1:g.126003G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1647G>A ENSP00000508434.1:n.*1647G>A
ENST00000440875.6:c.1021G>A ENSP00000475553.3:p.Glu341Lys
ENST00000627532.3:c.1798G>A MANE Select ENSP00000487174.1:p.Glu600Lys
ENST00000636026.2:c.1798G>A ENSP00000490776.1:p.Glu600Lys
ENST00000636179.1:n.1767G>A
ENST00000636413.1:c.1462G>A ENSP00000490508.1:p.Glu488Lys
ENST00000636471.1:c.1873G>A ENSP00000490317.1:p.Glu625Lys
ENST00000636732.2:c.*1515G>A ENSP00000490175.1:n.*1515G>A
ENST00000636820.1:n.1898G>A
ENST00000637045.1:c.1462G>A ENSP00000490141.1:p.Glu488Lys
ENST00000637267.2:c.1798G>A ENSP00000490293.2:p.Glu600Lys
ENST00000637304.1:c.1462G>A ENSP00000490872.1:p.Glu488Lys
ENST00000638007.1:c.1462G>A ENSP00000490723.1:p.Glu488Lys
ENST00000638087.1:c.1462G>A ENSP00000490673.1:p.Glu488Lys
ENST00000638128.1:c.1021G>A ENSP00000490934.1:p.Glu341Lys
ENST00000675069.1:c.-133-539G>A ENSP00000502467.1:n.-133-539G>A
ENST00000675145.1:n.2346G>A
ENST00000303660.8:c.1795G>A ENSP00000302501.4:p.Glu599Lys
ENST00000409487.7:c.1798G>A ENSP00000386854.2:p.Glu600Lys
ENST00000419938.5:c.655+1810G>A ENSP00000394777.2:n.655+1810G>A
ENST00000427902.5:c.1885G>A ENSP00000395496.2:p.Glu629Lys
ENST00000440875.5:c.1167+148G>A ENSP00000475553.2:n.1167+148G>A
ENST00000539609.7:c.1726G>A ENSP00000443792.2:p.Glu576Lys
ENST00000558170.6:c.1798G>A ENSP00000454157.1:p.Glu600Lys
ENST00000627532.2:c.1798G>A ENSP00000487174.1:p.Glu600Lys
NM_001171653.1:c.1726G>A NP_001165124.1:p.Glu576Lys
NM_014795.3:c.1798G>A NP_055610.1:p.Glu600Lys
XM_006712881.2:c.1798G>A XP_006712944.1:p.Glu600Lys
XM_006712882.2:c.1798G>A XP_006712945.1:p.Glu600Lys
XM_011512231.1:c.1789G>A XP_011510533.1:p.Glu597Lys
XM_011512232.1:c.1777G>A XP_011510534.1:p.Glu593Lys
NM_014795.4:c.1798G>A MANE Select NP_055610.1:p.Glu600Lys
NM_001171653.2:c.1726G>A NP_001165124.1:p.Glu576Lys