Canonical Allele Identifier: CA2580063952
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753118
ClinVar RCV Id: RCV002369089

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144404085_144404088dup , CM000664.2:g.144404085_144404088dup GRCh38
NC_000002.11:g.145161652_145161655dup , CM000664.1:g.145161652_145161655dup GRCh37
NC_000002.10:g.144878122_144878125dup NCBI36
NG_016431.1:g.121306_121309dup

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*486_*489dup ENSP00000508434.1:n.*486_*489dup
ENST00000440875.6:c.-141_-138dup ENSP00000475553.3:n.-141_-138dup
ENST00000627532.3:c.637_640dup MANE Select ENSP00000487174.1:p.Pro214LeufsTer26
ENST00000636026.2:c.637_640dup ENSP00000490776.1:p.Pro214LeufsTer26
ENST00000636179.1:n.606_609dup
ENST00000636413.1:c.301_304dup ENSP00000490508.1:p.Pro102LeufsTer26
ENST00000636471.1:c.637_640dup ENSP00000490317.1:p.Pro214LeufsTer26
ENST00000636732.2:c.*354_*357dup ENSP00000490175.1:n.*354_*357dup
ENST00000636820.1:n.737_740dup
ENST00000637045.1:c.301_304dup ENSP00000490141.1:p.Pro102LeufsTer26
ENST00000637267.2:c.637_640dup ENSP00000490293.2:p.Pro214LeufsTer26
ENST00000637304.1:c.301_304dup ENSP00000490872.1:p.Pro102LeufsTer26
ENST00000638007.1:c.301_304dup ENSP00000490723.1:p.Pro102LeufsTer26
ENST00000638087.1:c.301_304dup ENSP00000490673.1:p.Pro102LeufsTer26
ENST00000638128.1:c.-141_-138dup ENSP00000490934.1:n.-141_-138dup
ENST00000675069.1:c.-133-5236_-133-5233dup ENSP00000502467.1:n.-133-5236_-133-5233dup
ENST00000303660.8:c.634_637dup ENSP00000302501.4:p.Pro213LeufsTer26
ENST00000392861.6:c.721_724dup ENSP00000376601.3:p.Pro242LeufsTer26
ENST00000409487.7:c.637_640dup ENSP00000386854.2:p.Pro214LeufsTer26
ENST00000419938.5:c.376_379dup ENSP00000394777.2:p.Pro127LeufsTer26
ENST00000427902.5:c.724_727dup ENSP00000395496.2:p.Pro243LeufsTer26
ENST00000440875.5:c.622_625dup ENSP00000475553.2:p.Pro209LeufsTer26
ENST00000497268.1:n.583_586dup
ENST00000539609.7:c.565_568dup ENSP00000443792.2:p.Pro190LeufsTer26
ENST00000558170.6:c.637_640dup ENSP00000454157.1:p.Pro214LeufsTer26
ENST00000627532.2:c.637_640dup ENSP00000487174.1:p.Pro214LeufsTer26
NM_001171653.1:c.565_568dup NP_001165124.1:p.Pro190LeufsTer26
NM_014795.3:c.637_640dup NP_055610.1:p.Pro214LeufsTer26
XM_006712881.2:c.637_640dup XP_006712944.1:p.Pro214LeufsTer26
XM_006712882.2:c.637_640dup XP_006712945.1:p.Pro214LeufsTer26
XM_011512231.1:c.628_631dup XP_011510533.1:p.Pro211LeufsTer26
XM_011512232.1:c.616_619dup XP_011510534.1:p.Pro207LeufsTer26
NM_014795.4:c.637_640dup MANE Select NP_055610.1:p.Pro214LeufsTer26
NM_001171653.2:c.565_568dup NP_001165124.1:p.Pro190LeufsTer26