Canonical Allele Identifier: CA1898134
Gene: ZEB2 HGNC NCBI

Linked Data

dbSNP Id: rs763943264

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389829_144389846dup , CM000664.2:g.144389829_144389846dup GRCh38
NC_000002.11:g.145147396_145147413dup , CM000664.1:g.145147396_145147413dup GRCh37
NC_000002.10:g.144863866_144863883dup NCBI36
NG_016431.1:g.135547_135564dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3100_*3117dup ENSP00000508434.1:n.*3100_*3117dup
ENST00000440875.6:c.2474_2491dup ENSP00000475553.3:p.Glu830_Ala831insGluAlaGluGluArgGlu
ENST00000627532.3:c.3251_3268dup MANE Select ENSP00000487174.1:p.Glu1089_Ala1090insGluAlaGluGluArgGlu
ENST00000636026.2:c.3230+21_3230+38dup ENSP00000490776.1:n.3230+21_3230+38dup
ENST00000636179.1:n.3220_3237dup
ENST00000636413.1:c.2915_2932dup ENSP00000490508.1:p.Glu977_Ala978insGluAlaGluGluArgGlu
ENST00000636471.1:c.3326_3343dup ENSP00000490317.1:p.Glu1114_Ala1115insGluAlaGluGluArgGlu
ENST00000636732.2:c.*2968_*2985dup ENSP00000490175.1:n.*2968_*2985dup
ENST00000636820.1:n.3351_3368dup
ENST00000637045.1:c.2915_2932dup ENSP00000490141.1:p.Glu977_Ala978insGluAlaGluGluArgGlu
ENST00000637304.1:c.2915_2932dup ENSP00000490872.1:p.Glu977_Ala978insGluAlaGluGluArgGlu
ENST00000638007.1:c.2915_2932dup ENSP00000490723.1:p.Glu977_Ala978insGluAlaGluGluArgGlu
ENST00000638087.1:c.2915_2932dup ENSP00000490673.1:p.Glu977_Ala978insGluAlaGluGluArgGlu
ENST00000638128.1:c.2474_2491dup ENSP00000490934.1:p.Glu830_Ala831insGluAlaGluGluArgGlu
ENST00000639389.1:c.151+6567_151+6584dup ENSP00000492572.1:n.151+6567_151+6584dup
ENST00000647488.1:c.471_488dup ENSP00000494820.1:n.471_488dup
ENST00000675069.1:c.782_799dup ENSP00000502467.1:p.Glu266_Ala267insGluAlaGluGluArgGlu
ENST00000303660.8:c.3248_3265dup ENSP00000302501.4:p.Glu1088_Ala1089insGluAlaGluGluArgGlu
ENST00000409487.7:c.3251_3268dup ENSP00000386854.2:p.Glu1089_Ala1090insGluAlaGluGluArgGlu
ENST00000419938.5:c.656-963_656-946dup ENSP00000394777.2:n.656-963_656-946dup
ENST00000539609.7:c.3179_3196dup ENSP00000443792.2:p.Glu1065_Ala1066insGluAlaGluGluArgGlu
ENST00000558170.6:c.3251_3268dup ENSP00000454157.1:p.Glu1089_Ala1090insGluAlaGluGluArgGlu
ENST00000627532.2:c.3251_3268dup ENSP00000487174.1:p.Glu1089_Ala1090insGluAlaGluGluArgGlu
NM_001171653.1:c.3179_3196dup NP_001165124.1:p.Glu1065_Ala1066insGluAlaGluGluArgGlu
NM_014795.3:c.3251_3268dup NP_055610.1:p.Glu1089_Ala1090insGluAlaGluGluArgGlu
XM_006712881.2:c.3251_3268dup XP_006712944.1:p.Glu1089_Ala1090insGluAlaGluGluArgGlu
XM_006712882.2:c.3251_3268dup XP_006712945.1:p.Glu1089_Ala1090insGluAlaGluGluArgGlu
XM_011512231.1:c.3242_3259dup XP_011510533.1:p.Glu1086_Ala1087insGluAlaGluGluArgGlu
XM_011512232.1:c.3230_3247dup XP_011510534.1:p.Glu1082_Ala1083insGluAlaGluGluArgGlu
NM_014795.4:c.3251_3268dup MANE Select NP_055610.1:p.Glu1089_Ala1090insGluAlaGluGluArgGlu
NM_001171653.2:c.3179_3196dup NP_001165124.1:p.Glu1065_Ala1066insGluAlaGluGluArgGlu