Canonical Allele Identifier: CA1294881416
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144390016_144390019delinsTGTG , CM000664.2:g.144390016_144390019delinsTGTG GRCh38
NC_000002.11:g.145147583_145147586delinsTGTG , CM000664.1:g.145147583_145147586delinsTGTG GRCh37
NC_000002.10:g.144864053_144864056delinsTGTG NCBI36
NG_016431.1:g.135373_135376delinsCACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*2926_*2929delinsCACA ENSP00000508434.1:n.*2926_*2929delinsCACA
ENST00000440875.6:c.2300_2303delinsCACA ENSP00000475553.3:p.Pro767=
ENST00000627532.3:c.3077_3080delinsCACA MANE Select ENSP00000487174.1:p.Pro1026=
ENST00000636026.2:c.3077_3080delinsCACA ENSP00000490776.1:p.Pro1026=
ENST00000636179.1:n.3046_3049delinsCACA
ENST00000636413.1:c.2741_2744delinsCACA ENSP00000490508.1:p.Pro914=
ENST00000636471.1:c.3152_3155delinsCACA ENSP00000490317.1:p.Pro1051=
ENST00000636732.2:c.*2794_*2797delinsCACA ENSP00000490175.1:n.*2794_*2797delinsCACA
ENST00000636820.1:n.3177_3180delinsCACA
ENST00000637045.1:c.2741_2744delinsCACA ENSP00000490141.1:p.Pro914=
ENST00000637304.1:c.2741_2744delinsCACA ENSP00000490872.1:p.Pro914=
ENST00000638007.1:c.2741_2744delinsCACA ENSP00000490723.1:p.Pro914=
ENST00000638087.1:c.2741_2744delinsCACA ENSP00000490673.1:p.Pro914=
ENST00000638128.1:c.2300_2303delinsCACA ENSP00000490934.1:p.Pro767=
ENST00000639389.1:c.151+6393_151+6396delinsCACA ENSP00000492572.1:n.151+6393_151+6396delinsCACA
ENST00000647488.1:c.297_300delinsCACA ENSP00000494820.1:n.297_300delinsCACA
ENST00000675069.1:c.608_611delinsCACA ENSP00000502467.1:p.Pro203=
ENST00000303660.8:c.3074_3077delinsCACA ENSP00000302501.4:p.Pro1025=
ENST00000409487.7:c.3077_3080delinsCACA ENSP00000386854.2:p.Pro1026=
ENST00000419938.5:c.656-1137_656-1134delinsCACA ENSP00000394777.2:n.656-1137_656-1134delinsCACA
ENST00000539609.7:c.3005_3008delinsCACA ENSP00000443792.2:p.Pro1002=
ENST00000558170.6:c.3077_3080delinsCACA ENSP00000454157.1:p.Pro1026=
ENST00000627532.2:c.3077_3080delinsCACA ENSP00000487174.1:p.Pro1026=
NM_001171653.1:c.3005_3008delinsCACA NP_001165124.1:p.Pro1002=
NM_014795.3:c.3077_3080delinsCACA NP_055610.1:p.Pro1026=
XM_006712881.2:c.3077_3080delinsCACA XP_006712944.1:p.Pro1026=
XM_006712882.2:c.3077_3080delinsCACA XP_006712945.1:p.Pro1026=
XM_011512231.1:c.3068_3071delinsCACA XP_011510533.1:p.Pro1023=
XM_011512232.1:c.3056_3059delinsCACA XP_011510534.1:p.Pro1019=
NM_014795.4:c.3077_3080delinsCACA MANE Select NP_055610.1:p.Pro1026=
NM_001171653.2:c.3005_3008delinsCACA NP_001165124.1:p.Pro1002=