Canonical Allele Identifier: CA2573133274
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1454365
ClinVar RCV Id: RCV001939473
dbSNP Id: rs2149876649

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144398813dup , CM000664.2:g.144398813dup GRCh38
NC_000002.11:g.145156380dup , CM000664.1:g.145156380dup GRCh37
NC_000002.10:g.144872850dup NCBI36
NG_016431.1:g.126579dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2223dup ENSP00000508434.1:n.*2223dup
ENST00000440875.6:c.1597dup ENSP00000475553.3:p.Ser533PhefsTer3
ENST00000627532.3:c.2374dup MANE Select ENSP00000487174.1:p.Ser792PhefsTer3
ENST00000636026.2:c.2374dup ENSP00000490776.1:p.Ser792PhefsTer3
ENST00000636179.1:n.2343dup
ENST00000636413.1:c.2038dup ENSP00000490508.1:p.Ser680PhefsTer3
ENST00000636471.1:c.2449dup ENSP00000490317.1:p.Ser817PhefsTer3
ENST00000636732.2:c.*2091dup ENSP00000490175.1:n.*2091dup
ENST00000636820.1:n.2474dup
ENST00000637045.1:c.2038dup ENSP00000490141.1:p.Ser680PhefsTer3
ENST00000637304.1:c.2038dup ENSP00000490872.1:p.Ser680PhefsTer3
ENST00000638007.1:c.2038dup ENSP00000490723.1:p.Ser680PhefsTer3
ENST00000638087.1:c.2038dup ENSP00000490673.1:p.Ser680PhefsTer3
ENST00000638128.1:c.1597dup ENSP00000490934.1:p.Ser533PhefsTer3
ENST00000675069.1:c.-96dup ENSP00000502467.1:n.-96dup
ENST00000675145.1:n.2922dup
ENST00000303660.8:c.2371dup ENSP00000302501.4:p.Ser791PhefsTer3
ENST00000409487.7:c.2374dup ENSP00000386854.2:p.Ser792PhefsTer3
ENST00000419938.5:c.655+2386dup ENSP00000394777.2:n.655+2386dup
ENST00000440875.5:c.1167+724dup ENSP00000475553.2:n.1167+724dup
ENST00000539609.7:c.2302dup ENSP00000443792.2:p.Ser768PhefsTer3
ENST00000558170.6:c.2374dup ENSP00000454157.1:p.Ser792PhefsTer3
ENST00000627532.2:c.2374dup ENSP00000487174.1:p.Ser792PhefsTer3
NM_001171653.1:c.2302dup NP_001165124.1:p.Ser768PhefsTer3
NM_014795.3:c.2374dup NP_055610.1:p.Ser792PhefsTer3
XM_006712881.2:c.2374dup XP_006712944.1:p.Ser792PhefsTer3
XM_006712882.2:c.2374dup XP_006712945.1:p.Ser792PhefsTer3
XM_011512231.1:c.2365dup XP_011510533.1:p.Ser789PhefsTer3
XM_011512232.1:c.2353dup XP_011510534.1:p.Ser785PhefsTer3
NM_014795.4:c.2374dup MANE Select NP_055610.1:p.Ser792PhefsTer3
NM_001171653.2:c.2302dup NP_001165124.1:p.Ser768PhefsTer3