Canonical Allele Identifier: CA348708350
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398777T>C , CM000664.2:g.144398777T>C GRCh38
NC_000002.11:g.145156344T>C , CM000664.1:g.145156344T>C GRCh37
NC_000002.10:g.144872814T>C NCBI36
NG_016431.1:g.126615A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2259A>G ENSP00000508434.1:n.*2259A>G
ENST00000440875.6:c.1633A>G ENSP00000475553.3:p.Asn545Asp
ENST00000627532.3:c.2410A>G MANE Select ENSP00000487174.1:p.Asn804Asp
ENST00000636026.2:c.2410A>G ENSP00000490776.1:p.Asn804Asp
ENST00000636179.1:n.2379A>G
ENST00000636413.1:c.2074A>G ENSP00000490508.1:p.Asn692Asp
ENST00000636471.1:c.2485A>G ENSP00000490317.1:p.Asn829Asp
ENST00000636732.2:c.*2127A>G ENSP00000490175.1:n.*2127A>G
ENST00000636820.1:n.2510A>G
ENST00000637045.1:c.2074A>G ENSP00000490141.1:p.Asn692Asp
ENST00000637304.1:c.2074A>G ENSP00000490872.1:p.Asn692Asp
ENST00000638007.1:c.2074A>G ENSP00000490723.1:p.Asn692Asp
ENST00000638087.1:c.2074A>G ENSP00000490673.1:p.Asn692Asp
ENST00000638128.1:c.1633A>G ENSP00000490934.1:p.Asn545Asp
ENST00000675069.1:c.-60A>G ENSP00000502467.1:n.-60A>G
ENST00000675145.1:n.2958A>G
ENST00000303660.8:c.2407A>G ENSP00000302501.4:p.Asn803Asp
ENST00000409487.7:c.2410A>G ENSP00000386854.2:p.Asn804Asp
ENST00000419938.5:c.655+2422A>G ENSP00000394777.2:n.655+2422A>G
ENST00000440875.5:c.1167+760A>G ENSP00000475553.2:n.1167+760A>G
ENST00000539609.7:c.2338A>G ENSP00000443792.2:p.Asn780Asp
ENST00000558170.6:c.2410A>G ENSP00000454157.1:p.Asn804Asp
ENST00000627532.2:c.2410A>G ENSP00000487174.1:p.Asn804Asp
NM_001171653.1:c.2338A>G NP_001165124.1:p.Asn780Asp
NM_014795.3:c.2410A>G NP_055610.1:p.Asn804Asp
XM_006712881.2:c.2410A>G XP_006712944.1:p.Asn804Asp
XM_006712882.2:c.2410A>G XP_006712945.1:p.Asn804Asp
XM_011512231.1:c.2401A>G XP_011510533.1:p.Asn801Asp
XM_011512232.1:c.2389A>G XP_011510534.1:p.Asn797Asp
NM_014795.4:c.2410A>G MANE Select NP_055610.1:p.Asn804Asp
NM_001171653.2:c.2338A>G NP_001165124.1:p.Asn780Asp