Canonical Allele Identifier: CA1294885493
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399983C= , CM000664.2:g.144399983C= GRCh38
NC_000002.11:g.145157550C= , CM000664.1:g.145157550C= GRCh37
NC_000002.10:g.144874020C= NCBI36
NG_016431.1:g.125409G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1053G= ENSP00000508434.1:n.*1053G=
ENST00000440875.6:c.427G= ENSP00000475553.3:p.Val143=
ENST00000627532.3:c.1204G= MANE Select ENSP00000487174.1:p.Val402=
ENST00000636026.2:c.1204G= ENSP00000490776.1:p.Val402=
ENST00000636179.1:n.1173G=
ENST00000636413.1:c.868G= ENSP00000490508.1:p.Val290=
ENST00000636471.1:c.1279G= ENSP00000490317.1:p.Val427=
ENST00000636732.2:c.*921G= ENSP00000490175.1:n.*921G=
ENST00000636820.1:n.1304G=
ENST00000637045.1:c.868G= ENSP00000490141.1:p.Val290=
ENST00000637267.2:c.1204G= ENSP00000490293.2:p.Val402=
ENST00000637304.1:c.868G= ENSP00000490872.1:p.Val290=
ENST00000638007.1:c.868G= ENSP00000490723.1:p.Val290=
ENST00000638087.1:c.868G= ENSP00000490673.1:p.Val290=
ENST00000638128.1:c.427G= ENSP00000490934.1:p.Val143=
ENST00000675069.1:c.-133-1133G= ENSP00000502467.1:n.-133-1133G=
ENST00000675145.1:n.1752G=
ENST00000303660.8:c.1201G= ENSP00000302501.4:p.Val401=
ENST00000392861.6:c.1288G= ENSP00000376601.3:p.Val430=
ENST00000409487.7:c.1204G= ENSP00000386854.2:p.Val402=
ENST00000419938.5:c.655+1216G= ENSP00000394777.2:n.655+1216G=
ENST00000427902.5:c.1291G= ENSP00000395496.2:p.Val431=
ENST00000440875.5:c.1153+36G= ENSP00000475553.2:n.1153+36G=
ENST00000539609.7:c.1132G= ENSP00000443792.2:p.Val378=
ENST00000558170.6:c.1204G= ENSP00000454157.1:p.Val402=
ENST00000627532.2:c.1204G= ENSP00000487174.1:p.Val402=
NM_001171653.1:c.1132G= NP_001165124.1:p.Val378=
NM_014795.3:c.1204G= NP_055610.1:p.Val402=
XM_006712881.2:c.1204G= XP_006712944.1:p.Val402=
XM_006712882.2:c.1204G= XP_006712945.1:p.Val402=
XM_011512231.1:c.1195G= XP_011510533.1:p.Val399=
XM_011512232.1:c.1183G= XP_011510534.1:p.Val395=
NM_014795.4:c.1204G= MANE Select NP_055610.1:p.Val402=
NM_001171653.2:c.1132G= NP_001165124.1:p.Val378=