Canonical Allele Identifier: CA1294885448
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144399873G= , CM000664.2:g.144399873G= GRCh38
NC_000002.11:g.145157440G= , CM000664.1:g.145157440G= GRCh37
NC_000002.10:g.144873910G= NCBI36
NG_016431.1:g.125519C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000689298.1:c.*1163C= ENSP00000508434.1:n.*1163C=
ENST00000440875.6:c.537C= ENSP00000475553.3:p.His179=
ENST00000627532.3:c.1314C= MANE Select ENSP00000487174.1:p.His438=
ENST00000636026.2:c.1314C= ENSP00000490776.1:p.His438=
ENST00000636179.1:n.1283C=
ENST00000636413.1:c.978C= ENSP00000490508.1:p.His326=
ENST00000636471.1:c.1389C= ENSP00000490317.1:p.His463=
ENST00000636732.2:c.*1031C= ENSP00000490175.1:n.*1031C=
ENST00000636820.1:n.1414C=
ENST00000637045.1:c.978C= ENSP00000490141.1:p.His326=
ENST00000637267.2:c.1314C= ENSP00000490293.2:p.His438=
ENST00000637304.1:c.978C= ENSP00000490872.1:p.His326=
ENST00000638007.1:c.978C= ENSP00000490723.1:p.His326=
ENST00000638087.1:c.978C= ENSP00000490673.1:p.His326=
ENST00000638128.1:c.537C= ENSP00000490934.1:p.His179=
ENST00000675069.1:c.-133-1023C= ENSP00000502467.1:n.-133-1023C=
ENST00000675145.1:n.1862C=
ENST00000303660.8:c.1311C= ENSP00000302501.4:p.His437=
ENST00000392861.6:c.1398C= ENSP00000376601.3:p.His466=
ENST00000409487.7:c.1314C= ENSP00000386854.2:p.His438=
ENST00000419938.5:c.655+1326C= ENSP00000394777.2:n.655+1326C=
ENST00000427902.5:c.1401C= ENSP00000395496.2:p.His467=
ENST00000440875.5:c.1153+146C= ENSP00000475553.2:n.1153+146C=
ENST00000539609.7:c.1242C= ENSP00000443792.2:p.His414=
ENST00000558170.6:c.1314C= ENSP00000454157.1:p.His438=
ENST00000627532.2:c.1314C= ENSP00000487174.1:p.His438=
NM_001171653.1:c.1242C= NP_001165124.1:p.His414=
NM_014795.3:c.1314C= NP_055610.1:p.His438=
XM_006712881.2:c.1314C= XP_006712944.1:p.His438=
XM_006712882.2:c.1314C= XP_006712945.1:p.His438=
XM_011512231.1:c.1305C= XP_011510533.1:p.His435=
XM_011512232.1:c.1293C= XP_011510534.1:p.His431=
NM_014795.4:c.1314C= MANE Select NP_055610.1:p.His438=
NM_001171653.2:c.1242C= NP_001165124.1:p.His414=