Canonical Allele Identifier: CA348707838
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398593A>C , CM000664.2:g.144398593A>C GRCh38
NC_000002.11:g.145156160A>C , CM000664.1:g.145156160A>C GRCh37
NC_000002.10:g.144872630A>C NCBI36
NG_016431.1:g.126799T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2443T>G ENSP00000508434.1:n.*2443T>G
ENST00000440875.6:c.1817T>G ENSP00000475553.3:p.Ile606Ser
ENST00000627532.3:c.2594T>G MANE Select ENSP00000487174.1:p.Ile865Ser
ENST00000636026.2:c.2594T>G ENSP00000490776.1:p.Ile865Ser
ENST00000636179.1:n.2563T>G
ENST00000636413.1:c.2258T>G ENSP00000490508.1:p.Ile753Ser
ENST00000636471.1:c.2669T>G ENSP00000490317.1:p.Ile890Ser
ENST00000636732.2:c.*2311T>G ENSP00000490175.1:n.*2311T>G
ENST00000636820.1:n.2694T>G
ENST00000637045.1:c.2258T>G ENSP00000490141.1:p.Ile753Ser
ENST00000637304.1:c.2258T>G ENSP00000490872.1:p.Ile753Ser
ENST00000638007.1:c.2258T>G ENSP00000490723.1:p.Ile753Ser
ENST00000638087.1:c.2258T>G ENSP00000490673.1:p.Ile753Ser
ENST00000638128.1:c.1817T>G ENSP00000490934.1:p.Ile606Ser
ENST00000675069.1:c.125T>G ENSP00000502467.1:p.Ile42Ser
ENST00000303660.8:c.2591T>G ENSP00000302501.4:p.Ile864Ser
ENST00000409487.7:c.2594T>G ENSP00000386854.2:p.Ile865Ser
ENST00000419938.5:c.655+2606T>G ENSP00000394777.2:n.655+2606T>G
ENST00000440875.5:c.1168-665T>G ENSP00000475553.2:n.1168-665T>G
ENST00000539609.7:c.2522T>G ENSP00000443792.2:p.Ile841Ser
ENST00000558170.6:c.2594T>G ENSP00000454157.1:p.Ile865Ser
ENST00000627532.2:c.2594T>G ENSP00000487174.1:p.Ile865Ser
NM_001171653.1:c.2522T>G NP_001165124.1:p.Ile841Ser
NM_014795.3:c.2594T>G NP_055610.1:p.Ile865Ser
XM_006712881.2:c.2594T>G XP_006712944.1:p.Ile865Ser
XM_006712882.2:c.2594T>G XP_006712945.1:p.Ile865Ser
XM_011512231.1:c.2585T>G XP_011510533.1:p.Ile862Ser
XM_011512232.1:c.2573T>G XP_011510534.1:p.Ile858Ser
NM_014795.4:c.2594T>G MANE Select NP_055610.1:p.Ile865Ser
NM_001171653.2:c.2522T>G NP_001165124.1:p.Ile841Ser