Canonical Allele Identifier: CA348708295
Gene: ZEB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398753G>C , CM000664.2:g.144398753G>C GRCh38
NC_000002.11:g.145156320G>C , CM000664.1:g.145156320G>C GRCh37
NC_000002.10:g.144872790G>C NCBI36
NG_016431.1:g.126639C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2283C>G ENSP00000508434.1:n.*2283C>G
ENST00000440875.6:c.1657C>G ENSP00000475553.3:p.Gln553Glu
ENST00000627532.3:c.2434C>G MANE Select ENSP00000487174.1:p.Gln812Glu
ENST00000636026.2:c.2434C>G ENSP00000490776.1:p.Gln812Glu
ENST00000636179.1:n.2403C>G
ENST00000636413.1:c.2098C>G ENSP00000490508.1:p.Gln700Glu
ENST00000636471.1:c.2509C>G ENSP00000490317.1:p.Gln837Glu
ENST00000636732.2:c.*2151C>G ENSP00000490175.1:n.*2151C>G
ENST00000636820.1:n.2534C>G
ENST00000637045.1:c.2098C>G ENSP00000490141.1:p.Gln700Glu
ENST00000637304.1:c.2098C>G ENSP00000490872.1:p.Gln700Glu
ENST00000638007.1:c.2098C>G ENSP00000490723.1:p.Gln700Glu
ENST00000638087.1:c.2098C>G ENSP00000490673.1:p.Gln700Glu
ENST00000638128.1:c.1657C>G ENSP00000490934.1:p.Gln553Glu
ENST00000675069.1:c.-36C>G ENSP00000502467.1:n.-36C>G
ENST00000675145.1:n.2982C>G
ENST00000303660.8:c.2431C>G ENSP00000302501.4:p.Gln811Glu
ENST00000409487.7:c.2434C>G ENSP00000386854.2:p.Gln812Glu
ENST00000419938.5:c.655+2446C>G ENSP00000394777.2:n.655+2446C>G
ENST00000440875.5:c.1167+784C>G ENSP00000475553.2:n.1167+784C>G
ENST00000539609.7:c.2362C>G ENSP00000443792.2:p.Gln788Glu
ENST00000558170.6:c.2434C>G ENSP00000454157.1:p.Gln812Glu
ENST00000627532.2:c.2434C>G ENSP00000487174.1:p.Gln812Glu
NM_001171653.1:c.2362C>G NP_001165124.1:p.Gln788Glu
NM_014795.3:c.2434C>G NP_055610.1:p.Gln812Glu
XM_006712881.2:c.2434C>G XP_006712944.1:p.Gln812Glu
XM_006712882.2:c.2434C>G XP_006712945.1:p.Gln812Glu
XM_011512231.1:c.2425C>G XP_011510533.1:p.Gln809Glu
XM_011512232.1:c.2413C>G XP_011510534.1:p.Gln805Glu
NM_014795.4:c.2434C>G MANE Select NP_055610.1:p.Gln812Glu
NM_001171653.2:c.2362C>G NP_001165124.1:p.Gln788Glu