Canonical Allele Identifier: CA348711378
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399743C>A , CM000664.2:g.144399743C>A GRCh38
NC_000002.11:g.145157310C>A , CM000664.1:g.145157310C>A GRCh37
NC_000002.10:g.144873780C>A NCBI36
NG_016431.1:g.125649G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1293G>T ENSP00000508434.1:n.*1293G>T
ENST00000440875.6:c.667G>T ENSP00000475553.3:p.Glu223Ter
ENST00000627532.3:c.1444G>T MANE Select ENSP00000487174.1:p.Glu482Ter
ENST00000636026.2:c.1444G>T ENSP00000490776.1:p.Glu482Ter
ENST00000636179.1:n.1413G>T
ENST00000636413.1:c.1108G>T ENSP00000490508.1:p.Glu370Ter
ENST00000636471.1:c.1519G>T ENSP00000490317.1:p.Glu507Ter
ENST00000636732.2:c.*1161G>T ENSP00000490175.1:n.*1161G>T
ENST00000636820.1:n.1544G>T
ENST00000637045.1:c.1108G>T ENSP00000490141.1:p.Glu370Ter
ENST00000637267.2:c.1444G>T ENSP00000490293.2:p.Glu482Ter
ENST00000637304.1:c.1108G>T ENSP00000490872.1:p.Glu370Ter
ENST00000638007.1:c.1108G>T ENSP00000490723.1:p.Glu370Ter
ENST00000638087.1:c.1108G>T ENSP00000490673.1:p.Glu370Ter
ENST00000638128.1:c.667G>T ENSP00000490934.1:p.Glu223Ter
ENST00000675069.1:c.-133-893G>T ENSP00000502467.1:n.-133-893G>T
ENST00000675145.1:n.1992G>T
ENST00000303660.8:c.1441G>T ENSP00000302501.4:p.Glu481Ter
ENST00000409487.7:c.1444G>T ENSP00000386854.2:p.Glu482Ter
ENST00000419938.5:c.655+1456G>T ENSP00000394777.2:n.655+1456G>T
ENST00000427902.5:c.1531G>T ENSP00000395496.2:p.Glu511Ter
ENST00000440875.5:c.1154-193G>T ENSP00000475553.2:n.1154-193G>T
ENST00000539609.7:c.1372G>T ENSP00000443792.2:p.Glu458Ter
ENST00000558170.6:c.1444G>T ENSP00000454157.1:p.Glu482Ter
ENST00000627532.2:c.1444G>T ENSP00000487174.1:p.Glu482Ter
NM_001171653.1:c.1372G>T NP_001165124.1:p.Glu458Ter
NM_014795.3:c.1444G>T NP_055610.1:p.Glu482Ter
XM_006712881.2:c.1444G>T XP_006712944.1:p.Glu482Ter
XM_006712882.2:c.1444G>T XP_006712945.1:p.Glu482Ter
XM_011512231.1:c.1435G>T XP_011510533.1:p.Glu479Ter
XM_011512232.1:c.1423G>T XP_011510534.1:p.Glu475Ter
NM_014795.4:c.1444G>T MANE Select NP_055610.1:p.Glu482Ter
NM_001171653.2:c.1372G>T NP_001165124.1:p.Glu458Ter