Canonical Allele Identifier: CA348712339

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145157540G>T (hg19) ; chr2:g.144399973G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399973G>T , CM000664.2:g.144399973G>T	GRCh38
NC_000002.11:g.145157540G>T , CM000664.1:g.145157540G>T	GRCh37
NC_000002.10:g.144874010G>T	NCBI36
NG_016431.1:g.125419C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1063C>A	ENSP00000508434.1:n.*1063C>A
ENST00000440875.6:c.437C>A	ENSP00000475553.3:p.Ala146Asp
ENST00000627532.3:c.1214C>A MANE Select	ENSP00000487174.1:p.Ala405Asp
ENST00000636026.2:c.1214C>A	ENSP00000490776.1:p.Ala405Asp
ENST00000636179.1:n.1183C>A
ENST00000636413.1:c.878C>A	ENSP00000490508.1:p.Ala293Asp
ENST00000636471.1:c.1289C>A	ENSP00000490317.1:p.Ala430Asp
ENST00000636732.2:c.*931C>A	ENSP00000490175.1:n.*931C>A
ENST00000636820.1:n.1314C>A
ENST00000637045.1:c.878C>A	ENSP00000490141.1:p.Ala293Asp
ENST00000637267.2:c.1214C>A	ENSP00000490293.2:p.Ala405Asp
ENST00000637304.1:c.878C>A	ENSP00000490872.1:p.Ala293Asp
ENST00000638007.1:c.878C>A	ENSP00000490723.1:p.Ala293Asp
ENST00000638087.1:c.878C>A	ENSP00000490673.1:p.Ala293Asp
ENST00000638128.1:c.437C>A	ENSP00000490934.1:p.Ala146Asp
ENST00000675069.1:c.-133-1123C>A	ENSP00000502467.1:n.-133-1123C>A
ENST00000675145.1:n.1762C>A
ENST00000303660.8:c.1211C>A	ENSP00000302501.4:p.Ala404Asp
ENST00000392861.6:c.1298C>A	ENSP00000376601.3:p.Ala433Asp
ENST00000409487.7:c.1214C>A	ENSP00000386854.2:p.Ala405Asp
ENST00000419938.5:c.655+1226C>A	ENSP00000394777.2:n.655+1226C>A
ENST00000427902.5:c.1301C>A	ENSP00000395496.2:p.Ala434Asp
ENST00000440875.5:c.1153+46C>A	ENSP00000475553.2:n.1153+46C>A
ENST00000539609.7:c.1142C>A	ENSP00000443792.2:p.Ala381Asp
ENST00000558170.6:c.1214C>A	ENSP00000454157.1:p.Ala405Asp
ENST00000627532.2:c.1214C>A	ENSP00000487174.1:p.Ala405Asp
NM_001171653.1:c.1142C>A	NP_001165124.1:p.Ala381Asp
NM_014795.3:c.1214C>A	NP_055610.1:p.Ala405Asp
XM_006712881.2:c.1214C>A	XP_006712944.1:p.Ala405Asp
XM_006712882.2:c.1214C>A	XP_006712945.1:p.Ala405Asp
XM_011512231.1:c.1205C>A	XP_011510533.1:p.Ala402Asp
XM_011512232.1:c.1193C>A	XP_011510534.1:p.Ala398Asp
NM_014795.4:c.1214C>A MANE Select	NP_055610.1:p.Ala405Asp
NM_001171653.2:c.1142C>A	NP_001165124.1:p.Ala381Asp