Canonical Allele Identifier: CA348707693
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398558T>A , CM000664.2:g.144398558T>A GRCh38
NC_000002.11:g.145156125T>A , CM000664.1:g.145156125T>A GRCh37
NC_000002.10:g.144872595T>A NCBI36
NG_016431.1:g.126834A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2478A>T ENSP00000508434.1:n.*2478A>T
ENST00000440875.6:c.1852A>T ENSP00000475553.3:p.Asn618Tyr
ENST00000627532.3:c.2629A>T MANE Select ENSP00000487174.1:p.Asn877Tyr
ENST00000636026.2:c.2629A>T ENSP00000490776.1:p.Asn877Tyr
ENST00000636179.1:n.2598A>T
ENST00000636413.1:c.2293A>T ENSP00000490508.1:p.Asn765Tyr
ENST00000636471.1:c.2704A>T ENSP00000490317.1:p.Asn902Tyr
ENST00000636732.2:c.*2346A>T ENSP00000490175.1:n.*2346A>T
ENST00000636820.1:n.2729A>T
ENST00000637045.1:c.2293A>T ENSP00000490141.1:p.Asn765Tyr
ENST00000637304.1:c.2293A>T ENSP00000490872.1:p.Asn765Tyr
ENST00000638007.1:c.2293A>T ENSP00000490723.1:p.Asn765Tyr
ENST00000638087.1:c.2293A>T ENSP00000490673.1:p.Asn765Tyr
ENST00000638128.1:c.1852A>T ENSP00000490934.1:p.Asn618Tyr
ENST00000675069.1:c.160A>T ENSP00000502467.1:p.Asn54Tyr
ENST00000303660.8:c.2626A>T ENSP00000302501.4:p.Asn876Tyr
ENST00000409487.7:c.2629A>T ENSP00000386854.2:p.Asn877Tyr
ENST00000419938.5:c.655+2641A>T ENSP00000394777.2:n.655+2641A>T
ENST00000440875.5:c.1168-630A>T ENSP00000475553.2:n.1168-630A>T
ENST00000539609.7:c.2557A>T ENSP00000443792.2:p.Asn853Tyr
ENST00000558170.6:c.2629A>T ENSP00000454157.1:p.Asn877Tyr
ENST00000627532.2:c.2629A>T ENSP00000487174.1:p.Asn877Tyr
NM_001171653.1:c.2557A>T NP_001165124.1:p.Asn853Tyr
NM_014795.3:c.2629A>T NP_055610.1:p.Asn877Tyr
XM_006712881.2:c.2629A>T XP_006712944.1:p.Asn877Tyr
XM_006712882.2:c.2629A>T XP_006712945.1:p.Asn877Tyr
XM_011512231.1:c.2620A>T XP_011510533.1:p.Asn874Tyr
XM_011512232.1:c.2608A>T XP_011510534.1:p.Asn870Tyr
NM_014795.4:c.2629A>T MANE Select NP_055610.1:p.Asn877Tyr
NM_001171653.2:c.2557A>T NP_001165124.1:p.Asn853Tyr