Canonical Allele Identifier: CA1294881399
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144389962T= , CM000664.2:g.144389962T= GRCh38
NC_000002.11:g.145147529T= , CM000664.1:g.145147529T= GRCh37
NC_000002.10:g.144863999T= NCBI36
NG_016431.1:g.135430A=

Transcript Alleles

HGVS Amino-acid Change
NM_014795.4:c.3134A= MANE Select NP_055610.1:p.His1045=
ENST00000627532.3:c.3134A= MANE Select ENSP00000487174.1:p.His1045=
NM_001171653.1:c.3062A= NP_001165124.1:p.His1021=
NM_001171653.2:c.3062A= NP_001165124.1:p.His1021=
NM_014795.3:c.3134A= NP_055610.1:p.His1045=
ENST00000303660.8:c.3131A= ENSP00000302501.4:p.His1044=
ENST00000409487.7:c.3134A= ENSP00000386854.2:p.His1045=
ENST00000419938.5:c.656-1080A= ENSP00000394777.2:n.656-1080A=
ENST00000440875.6:c.2357A= ENSP00000475553.3:p.His786=
ENST00000539609.7:c.3062A= ENSP00000443792.2:p.His1021=
ENST00000558170.6:c.3134A= ENSP00000454157.1:p.His1045=
ENST00000627532.2:c.3134A= ENSP00000487174.1:p.His1045=
ENST00000636026.2:c.3134A= ENSP00000490776.1:p.His1045=
ENST00000636179.1:n.3103A=
ENST00000636413.1:c.2798A= ENSP00000490508.1:p.His933=
ENST00000636471.1:c.3209A= ENSP00000490317.1:p.His1070=
ENST00000636732.2:c.*2851A= ENSP00000490175.1:n.*2851A=
ENST00000636820.1:n.3234A=
ENST00000637045.1:c.2798A= ENSP00000490141.1:p.His933=
ENST00000637304.1:c.2798A= ENSP00000490872.1:p.His933=
ENST00000638007.1:c.2798A= ENSP00000490723.1:p.His933=
ENST00000638087.1:c.2798A= ENSP00000490673.1:p.His933=
ENST00000638128.1:c.2357A= ENSP00000490934.1:p.His786=
ENST00000639389.1:c.151+6450A= ENSP00000492572.1:n.151+6450A=
ENST00000647488.1:c.354A= ENSP00000494820.1:n.354A=
ENST00000675069.1:c.665A= ENSP00000502467.1:p.His222=
ENST00000689298.1:c.*2983A= ENSP00000508434.1:n.*2983A=
XM_006712881.2:c.3134A= XP_006712944.1:p.His1045=
XM_006712882.2:c.3134A= XP_006712945.1:p.His1045=
XM_011512231.1:c.3125A= XP_011510533.1:p.His1042=
XM_011512232.1:c.3113A= XP_011510534.1:p.His1038=