Canonical Allele Identifier: CA267212
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399010_144399013dup , CM000664.2:g.144399010_144399013dup GRCh38
NC_000002.11:g.145156577_145156580dup , CM000664.1:g.145156577_145156580dup GRCh37
NC_000002.10:g.144873047_144873050dup NCBI36
NG_016431.1:g.126379_126382dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2023_*2026dup ENSP00000508434.1:n.*2023_*2026dup
ENST00000440875.6:c.1397_1400dup ENSP00000475553.3:p.Leu469PhefsTer29
ENST00000627532.3:c.2174_2177dup MANE Select ENSP00000487174.1:p.Leu728PhefsTer29
ENST00000636026.2:c.2174_2177dup ENSP00000490776.1:p.Leu728PhefsTer29
ENST00000636179.1:n.2143_2146dup
ENST00000636413.1:c.1838_1841dup ENSP00000490508.1:p.Leu616PhefsTer29
ENST00000636471.1:c.2249_2252dup ENSP00000490317.1:p.Leu753PhefsTer29
ENST00000636732.2:c.*1891_*1894dup ENSP00000490175.1:n.*1891_*1894dup
ENST00000636820.1:n.2274_2277dup
ENST00000637045.1:c.1838_1841dup ENSP00000490141.1:p.Leu616PhefsTer29
ENST00000637304.1:c.1838_1841dup ENSP00000490872.1:p.Leu616PhefsTer29
ENST00000638007.1:c.1838_1841dup ENSP00000490723.1:p.Leu616PhefsTer29
ENST00000638087.1:c.1838_1841dup ENSP00000490673.1:p.Leu616PhefsTer29
ENST00000638128.1:c.1397_1400dup ENSP00000490934.1:p.Leu469PhefsTer29
ENST00000675069.1:c.-133-163_-133-160dup ENSP00000502467.1:n.-133-163_-133-160dup
ENST00000675145.1:n.2722_2725dup
ENST00000303660.8:c.2171_2174dup ENSP00000302501.4:p.Leu727PhefsTer29
ENST00000409487.7:c.2174_2177dup ENSP00000386854.2:p.Leu728PhefsTer29
ENST00000419938.5:c.655+2186_655+2189dup ENSP00000394777.2:n.655+2186_655+2189dup
ENST00000440875.5:c.1167+524_1167+527dup ENSP00000475553.2:n.1167+524_1167+527dup
ENST00000539609.7:c.2102_2105dup ENSP00000443792.2:p.Leu704PhefsTer29
ENST00000558170.6:c.2174_2177dup ENSP00000454157.1:p.Leu728PhefsTer29
ENST00000627532.2:c.2174_2177dup ENSP00000487174.1:p.Leu728PhefsTer29
NM_001171653.1:c.2102_2105dup NP_001165124.1:p.Leu704PhefsTer29
NM_014795.3:c.2174_2177dup NP_055610.1:p.Leu728PhefsTer29
XM_006712881.2:c.2174_2177dup XP_006712944.1:p.Leu728PhefsTer29
XM_006712882.2:c.2174_2177dup XP_006712945.1:p.Leu728PhefsTer29
XM_011512231.1:c.2165_2168dup XP_011510533.1:p.Leu725PhefsTer29
XM_011512232.1:c.2153_2156dup XP_011510534.1:p.Leu721PhefsTer29
NM_014795.4:c.2174_2177dup MANE Select NP_055610.1:p.Leu728PhefsTer29
NM_001171653.2:c.2102_2105dup NP_001165124.1:p.Leu704PhefsTer29