Canonical Allele Identifier: CA348714903
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144404072G>T , CM000664.2:g.144404072G>T GRCh38
NC_000002.11:g.145161639G>T , CM000664.1:g.145161639G>T GRCh37
NC_000002.10:g.144878109G>T NCBI36
NG_016431.1:g.121320C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*500C>A ENSP00000508434.1:n.*500C>A
ENST00000440875.6:c.-127C>A ENSP00000475553.3:n.-127C>A
ENST00000627532.3:c.651C>A MANE Select ENSP00000487174.1:p.Asp217Glu
ENST00000636026.2:c.651C>A ENSP00000490776.1:p.Asp217Glu
ENST00000636179.1:n.620C>A
ENST00000636413.1:c.315C>A ENSP00000490508.1:p.Asp105Glu
ENST00000636471.1:c.651C>A ENSP00000490317.1:p.Asp217Glu
ENST00000636732.2:c.*368C>A ENSP00000490175.1:n.*368C>A
ENST00000636820.1:n.751C>A
ENST00000637045.1:c.315C>A ENSP00000490141.1:p.Asp105Glu
ENST00000637267.2:c.651C>A ENSP00000490293.2:p.Asp217Glu
ENST00000637304.1:c.315C>A ENSP00000490872.1:p.Asp105Glu
ENST00000638007.1:c.315C>A ENSP00000490723.1:p.Asp105Glu
ENST00000638087.1:c.315C>A ENSP00000490673.1:p.Asp105Glu
ENST00000638128.1:c.-127C>A ENSP00000490934.1:n.-127C>A
ENST00000675069.1:c.-133-5222C>A ENSP00000502467.1:n.-133-5222C>A
ENST00000303660.8:c.648C>A ENSP00000302501.4:p.Asp216Glu
ENST00000392861.6:c.735C>A ENSP00000376601.3:p.Asp245Glu
ENST00000409487.7:c.651C>A ENSP00000386854.2:p.Asp217Glu
ENST00000419938.5:c.390C>A ENSP00000394777.2:p.Asp130Glu
ENST00000427902.5:c.738C>A ENSP00000395496.2:p.Asp246Glu
ENST00000440875.5:c.636C>A ENSP00000475553.2:p.Asp212Glu
ENST00000497268.1:n.597C>A
ENST00000539609.7:c.579C>A ENSP00000443792.2:p.Asp193Glu
ENST00000558170.6:c.651C>A ENSP00000454157.1:p.Asp217Glu
ENST00000627532.2:c.651C>A ENSP00000487174.1:p.Asp217Glu
NM_001171653.1:c.579C>A NP_001165124.1:p.Asp193Glu
NM_014795.3:c.651C>A NP_055610.1:p.Asp217Glu
XM_006712881.2:c.651C>A XP_006712944.1:p.Asp217Glu
XM_006712882.2:c.651C>A XP_006712945.1:p.Asp217Glu
XM_011512231.1:c.642C>A XP_011510533.1:p.Asp214Glu
XM_011512232.1:c.630C>A XP_011510534.1:p.Asp210Glu
NM_014795.4:c.651C>A MANE Select NP_055610.1:p.Asp217Glu
NM_001171653.2:c.579C>A NP_001165124.1:p.Asp193Glu