Canonical Allele Identifier: CA348711375
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399742T>G , CM000664.2:g.144399742T>G GRCh38
NC_000002.11:g.145157309T>G , CM000664.1:g.145157309T>G GRCh37
NC_000002.10:g.144873779T>G NCBI36
NG_016431.1:g.125650A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1294A>C ENSP00000508434.1:n.*1294A>C
ENST00000440875.6:c.668A>C ENSP00000475553.3:p.Glu223Ala
ENST00000627532.3:c.1445A>C MANE Select ENSP00000487174.1:p.Glu482Ala
ENST00000636026.2:c.1445A>C ENSP00000490776.1:p.Glu482Ala
ENST00000636179.1:n.1414A>C
ENST00000636413.1:c.1109A>C ENSP00000490508.1:p.Glu370Ala
ENST00000636471.1:c.1520A>C ENSP00000490317.1:p.Glu507Ala
ENST00000636732.2:c.*1162A>C ENSP00000490175.1:n.*1162A>C
ENST00000636820.1:n.1545A>C
ENST00000637045.1:c.1109A>C ENSP00000490141.1:p.Glu370Ala
ENST00000637267.2:c.1445A>C ENSP00000490293.2:p.Glu482Ala
ENST00000637304.1:c.1109A>C ENSP00000490872.1:p.Glu370Ala
ENST00000638007.1:c.1109A>C ENSP00000490723.1:p.Glu370Ala
ENST00000638087.1:c.1109A>C ENSP00000490673.1:p.Glu370Ala
ENST00000638128.1:c.668A>C ENSP00000490934.1:p.Glu223Ala
ENST00000675069.1:c.-133-892A>C ENSP00000502467.1:n.-133-892A>C
ENST00000675145.1:n.1993A>C
ENST00000303660.8:c.1442A>C ENSP00000302501.4:p.Glu481Ala
ENST00000409487.7:c.1445A>C ENSP00000386854.2:p.Glu482Ala
ENST00000419938.5:c.655+1457A>C ENSP00000394777.2:n.655+1457A>C
ENST00000427902.5:c.1532A>C ENSP00000395496.2:p.Glu511Ala
ENST00000440875.5:c.1154-192A>C ENSP00000475553.2:n.1154-192A>C
ENST00000539609.7:c.1373A>C ENSP00000443792.2:p.Glu458Ala
ENST00000558170.6:c.1445A>C ENSP00000454157.1:p.Glu482Ala
ENST00000627532.2:c.1445A>C ENSP00000487174.1:p.Glu482Ala
NM_001171653.1:c.1373A>C NP_001165124.1:p.Glu458Ala
NM_014795.3:c.1445A>C NP_055610.1:p.Glu482Ala
XM_006712881.2:c.1445A>C XP_006712944.1:p.Glu482Ala
XM_006712882.2:c.1445A>C XP_006712945.1:p.Glu482Ala
XM_011512231.1:c.1436A>C XP_011510533.1:p.Glu479Ala
XM_011512232.1:c.1424A>C XP_011510534.1:p.Glu475Ala
NM_014795.4:c.1445A>C MANE Select NP_055610.1:p.Glu482Ala
NM_001171653.2:c.1373A>C NP_001165124.1:p.Glu458Ala