Canonical Allele Identifier: CA267209
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399647dup , CM000664.2:g.144399647dup GRCh38
NC_000002.11:g.145157214dup , CM000664.1:g.145157214dup GRCh37
NC_000002.10:g.144873684dup NCBI36
NG_016431.1:g.125746dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1390dup ENSP00000508434.1:n.*1390dup
ENST00000440875.6:c.764dup ENSP00000475553.3:p.Val256GlyfsTer5
ENST00000627532.3:c.1541dup MANE Select ENSP00000487174.1:p.Val515GlyfsTer5
ENST00000636026.2:c.1541dup ENSP00000490776.1:p.Val515GlyfsTer5
ENST00000636179.1:n.1510dup
ENST00000636413.1:c.1205dup ENSP00000490508.1:p.Val403GlyfsTer5
ENST00000636471.1:c.1616dup ENSP00000490317.1:p.Val540GlyfsTer5
ENST00000636732.2:c.*1258dup ENSP00000490175.1:n.*1258dup
ENST00000636820.1:n.1641dup
ENST00000637045.1:c.1205dup ENSP00000490141.1:p.Val403GlyfsTer5
ENST00000637267.2:c.1541dup ENSP00000490293.2:p.Val515GlyfsTer5
ENST00000637304.1:c.1205dup ENSP00000490872.1:p.Val403GlyfsTer5
ENST00000638007.1:c.1205dup ENSP00000490723.1:p.Val403GlyfsTer5
ENST00000638087.1:c.1205dup ENSP00000490673.1:p.Val403GlyfsTer5
ENST00000638128.1:c.764dup ENSP00000490934.1:p.Val256GlyfsTer5
ENST00000675069.1:c.-133-796dup ENSP00000502467.1:n.-133-796dup
ENST00000675145.1:n.2089dup
ENST00000303660.8:c.1538dup ENSP00000302501.4:p.Val514GlyfsTer5
ENST00000409487.7:c.1541dup ENSP00000386854.2:p.Val515GlyfsTer5
ENST00000419938.5:c.655+1553dup ENSP00000394777.2:n.655+1553dup
ENST00000427902.5:c.1628dup ENSP00000395496.2:p.Val544GlyfsTer5
ENST00000440875.5:c.1154-96dup ENSP00000475553.2:n.1154-96dup
ENST00000539609.7:c.1469dup ENSP00000443792.2:p.Val491GlyfsTer5
ENST00000558170.6:c.1541dup ENSP00000454157.1:p.Val515GlyfsTer5
ENST00000627532.2:c.1541dup ENSP00000487174.1:p.Val515GlyfsTer5
NM_001171653.1:c.1469dup NP_001165124.1:p.Val491GlyfsTer5
NM_014795.3:c.1541dup NP_055610.1:p.Val515GlyfsTer5
XM_006712881.2:c.1541dup XP_006712944.1:p.Val515GlyfsTer5
XM_006712882.2:c.1541dup XP_006712945.1:p.Val515GlyfsTer5
XM_011512231.1:c.1532dup XP_011510533.1:p.Val512GlyfsTer5
XM_011512232.1:c.1520dup XP_011510534.1:p.Val508GlyfsTer5
NM_014795.4:c.1541dup MANE Select NP_055610.1:p.Val515GlyfsTer5
NM_001171653.2:c.1469dup NP_001165124.1:p.Val491GlyfsTer5