Canonical Allele Identifier: CA2586969977
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389623_144389624dup , CM000664.2:g.144389623_144389624dup GRCh38
NC_000002.11:g.145147190_145147191dup , CM000664.1:g.145147190_145147191dup GRCh37
NC_000002.10:g.144863660_144863661dup NCBI36
NG_016431.1:g.135769_135770dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*3322_*3323dup ENSP00000508434.1:n.*3322_*3323dup
ENST00000440875.6:c.2696_2697dup ENSP00000475553.3:p.Glu900ArgfsTer?
ENST00000627532.3:c.3473_3474dup MANE Select ENSP00000487174.1:p.Glu1159ArgfsTer?
ENST00000636026.2:c.3361_3362dup ENSP00000490776.1:p.Ser1122GlyfsTer10
ENST00000636179.1:n.3442_3443dup
ENST00000636413.1:c.3137_3138dup ENSP00000490508.1:p.Glu1047ArgfsTer?
ENST00000636471.1:c.3548_3549dup ENSP00000490317.1:p.Glu1184ArgfsTer?
ENST00000636732.2:c.*3190_*3191dup ENSP00000490175.1:n.*3190_*3191dup
ENST00000636820.1:n.3573_3574dup
ENST00000637045.1:c.3137_3138dup ENSP00000490141.1:p.Glu1047ArgfsTer?
ENST00000637304.1:c.3137_3138dup ENSP00000490872.1:p.Glu1047ArgfsTer?
ENST00000638007.1:c.3137_3138dup ENSP00000490723.1:p.Glu1047ArgfsTer?
ENST00000638087.1:c.3137_3138dup ENSP00000490673.1:p.Glu1047ArgfsTer?
ENST00000638128.1:c.2696_2697dup ENSP00000490934.1:p.Glu900ArgfsTer?
ENST00000639389.1:c.151+6789_151+6790dup ENSP00000492572.1:n.151+6789_151+6790dup
ENST00000647488.1:c.693_694dup ENSP00000494820.1:n.693_694dup
ENST00000675069.1:c.1004_1005dup ENSP00000502467.1:p.Glu336ArgfsTer?
ENST00000303660.8:c.3470_3471dup ENSP00000302501.4:p.Glu1158ArgfsTer?
ENST00000409487.7:c.3473_3474dup ENSP00000386854.2:p.Glu1159ArgfsTer?
ENST00000419938.5:c.656-741_656-740dup ENSP00000394777.2:n.656-741_656-740dup
ENST00000539609.7:c.3401_3402dup ENSP00000443792.2:p.Glu1135ArgfsTer?
ENST00000558170.6:c.3473_3474dup ENSP00000454157.1:p.Glu1159ArgfsTer?
ENST00000627532.2:c.3473_3474dup ENSP00000487174.1:p.Glu1159ArgfsTer?
NM_001171653.1:c.3401_3402dup NP_001165124.1:p.Glu1135ArgfsTer?
NM_014795.3:c.3473_3474dup NP_055610.1:p.Glu1159ArgfsTer?
XM_006712881.2:c.3473_3474dup XP_006712944.1:p.Glu1159ArgfsTer?
XM_006712882.2:c.3473_3474dup XP_006712945.1:p.Glu1159ArgfsTer?
XM_011512231.1:c.3464_3465dup XP_011510533.1:p.Glu1156ArgfsTer?
XM_011512232.1:c.3452_3453dup XP_011510534.1:p.Glu1152ArgfsTer?
NM_014795.4:c.3473_3474dup MANE Select NP_055610.1:p.Glu1159ArgfsTer?
NM_001171653.2:c.3401_3402dup NP_001165124.1:p.Glu1135ArgfsTer?