Canonical Allele Identifier: CA348707520
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398522A>T , CM000664.2:g.144398522A>T GRCh38
NC_000002.11:g.145156089A>T , CM000664.1:g.145156089A>T GRCh37
NC_000002.10:g.144872559A>T NCBI36
NG_016431.1:g.126870T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2514T>A ENSP00000508434.1:n.*2514T>A
ENST00000440875.6:c.1888T>A ENSP00000475553.3:p.Phe630Ile
ENST00000627532.3:c.2665T>A MANE Select ENSP00000487174.1:p.Phe889Ile
ENST00000636026.2:c.2665T>A ENSP00000490776.1:p.Phe889Ile
ENST00000636179.1:n.2634T>A
ENST00000636413.1:c.2329T>A ENSP00000490508.1:p.Phe777Ile
ENST00000636471.1:c.2740T>A ENSP00000490317.1:p.Phe914Ile
ENST00000636732.2:c.*2382T>A ENSP00000490175.1:n.*2382T>A
ENST00000636820.1:n.2765T>A
ENST00000637045.1:c.2329T>A ENSP00000490141.1:p.Phe777Ile
ENST00000637304.1:c.2329T>A ENSP00000490872.1:p.Phe777Ile
ENST00000638007.1:c.2329T>A ENSP00000490723.1:p.Phe777Ile
ENST00000638087.1:c.2329T>A ENSP00000490673.1:p.Phe777Ile
ENST00000638128.1:c.1888T>A ENSP00000490934.1:p.Phe630Ile
ENST00000675069.1:c.196T>A ENSP00000502467.1:p.Phe66Ile
ENST00000303660.8:c.2662T>A ENSP00000302501.4:p.Phe888Ile
ENST00000409487.7:c.2665T>A ENSP00000386854.2:p.Phe889Ile
ENST00000419938.5:c.655+2677T>A ENSP00000394777.2:n.655+2677T>A
ENST00000440875.5:c.1168-594T>A ENSP00000475553.2:n.1168-594T>A
ENST00000539609.7:c.2593T>A ENSP00000443792.2:p.Phe865Ile
ENST00000558170.6:c.2665T>A ENSP00000454157.1:p.Phe889Ile
ENST00000627532.2:c.2665T>A ENSP00000487174.1:p.Phe889Ile
NM_001171653.1:c.2593T>A NP_001165124.1:p.Phe865Ile
NM_014795.3:c.2665T>A NP_055610.1:p.Phe889Ile
XM_006712881.2:c.2665T>A XP_006712944.1:p.Phe889Ile
XM_006712882.2:c.2665T>A XP_006712945.1:p.Phe889Ile
XM_011512231.1:c.2656T>A XP_011510533.1:p.Phe886Ile
XM_011512232.1:c.2644T>A XP_011510534.1:p.Phe882Ile
NM_014795.4:c.2665T>A MANE Select NP_055610.1:p.Phe889Ile
NM_001171653.2:c.2593T>A NP_001165124.1:p.Phe865Ile