Canonical Allele Identifier: CA348704840
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144396573G>A , CM000664.2:g.144396573G>A GRCh38
NC_000002.11:g.145154140G>A , CM000664.1:g.145154140G>A GRCh37
NC_000002.10:g.144870610G>A NCBI36
NG_016431.1:g.128819C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*2755C>T ENSP00000508434.1:n.*2755C>T
ENST00000440875.6:c.2129C>T ENSP00000475553.3:p.Ala710Val
ENST00000627532.3:c.2906C>T MANE Select ENSP00000487174.1:p.Ala969Val
ENST00000636026.2:c.2906C>T ENSP00000490776.1:p.Ala969Val
ENST00000636179.1:n.2875C>T
ENST00000636413.1:c.2570C>T ENSP00000490508.1:p.Ala857Val
ENST00000636471.1:c.2981C>T ENSP00000490317.1:p.Ala994Val
ENST00000636732.2:c.*2623C>T ENSP00000490175.1:n.*2623C>T
ENST00000636820.1:n.3006C>T
ENST00000637045.1:c.2570C>T ENSP00000490141.1:p.Ala857Val
ENST00000637304.1:c.2570C>T ENSP00000490872.1:p.Ala857Val
ENST00000638007.1:c.2570C>T ENSP00000490723.1:p.Ala857Val
ENST00000638087.1:c.2570C>T ENSP00000490673.1:p.Ala857Val
ENST00000638128.1:c.2129C>T ENSP00000490934.1:p.Ala710Val
ENST00000647488.1:c.38C>T ENSP00000494820.1:p.Ala13Val
ENST00000675069.1:c.437C>T ENSP00000502467.1:p.Ala146Val
ENST00000303660.8:c.2903C>T ENSP00000302501.4:p.Ala968Val
ENST00000409487.7:c.2906C>T ENSP00000386854.2:p.Ala969Val
ENST00000419938.5:c.655+4626C>T ENSP00000394777.2:n.655+4626C>T
ENST00000539609.7:c.2834C>T ENSP00000443792.2:p.Ala945Val
ENST00000558170.6:c.2906C>T ENSP00000454157.1:p.Ala969Val
ENST00000627532.2:c.2906C>T ENSP00000487174.1:p.Ala969Val
NM_001171653.1:c.2834C>T NP_001165124.1:p.Ala945Val
NM_014795.3:c.2906C>T NP_055610.1:p.Ala969Val
XM_006712881.2:c.2906C>T XP_006712944.1:p.Ala969Val
XM_006712882.2:c.2906C>T XP_006712945.1:p.Ala969Val
XM_011512231.1:c.2897C>T XP_011510533.1:p.Ala966Val
XM_011512232.1:c.2885C>T XP_011510534.1:p.Ala962Val
NM_014795.4:c.2906C>T MANE Select NP_055610.1:p.Ala969Val
NM_001171653.2:c.2834C>T NP_001165124.1:p.Ala945Val