Canonical Allele Identifier: CA1294885969
Community Standard Title: NM_014795.4(ZEB2):c.904C= (p.Arg302=)
Gene: ZEB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144401211G= , CM000664.2:g.144401211G= GRCh38
NC_000002.11:g.145158778G= , CM000664.1:g.145158778G= GRCh37
NC_000002.10:g.144875248G= NCBI36
NG_016431.1:g.124181C=

Transcript Alleles

HGVS Amino-acid Change
NM_014795.4:c.904C= MANE Select NP_055610.1:p.Arg302=
ENST00000627532.3:c.904C= MANE Select ENSP00000487174.1:p.Arg302=
NM_001171653.1:c.832C= NP_001165124.1:p.Arg278=
NM_001171653.2:c.832C= NP_001165124.1:p.Arg278=
NM_014795.3:c.904C= NP_055610.1:p.Arg302=
ENST00000303660.8:c.901C= ENSP00000302501.4:p.Arg301=
ENST00000392861.6:c.988C= ENSP00000376601.3:p.Arg330=
ENST00000409487.7:c.904C= ENSP00000386854.2:p.Arg302=
ENST00000419938.5:c.643C= ENSP00000394777.2:p.Arg215=
ENST00000427902.5:c.991C= ENSP00000395496.2:p.Arg331=
ENST00000440875.5:c.889C= ENSP00000475553.2:p.Arg297=
ENST00000440875.6:c.127C= ENSP00000475553.3:p.Arg43=
ENST00000539609.7:c.832C= ENSP00000443792.2:p.Arg278=
ENST00000558170.6:c.904C= ENSP00000454157.1:p.Arg302=
ENST00000627532.2:c.904C= ENSP00000487174.1:p.Arg302=
ENST00000636026.2:c.904C= ENSP00000490776.1:p.Arg302=
ENST00000636179.1:n.873C=
ENST00000636413.1:c.568C= ENSP00000490508.1:p.Arg190=
ENST00000636471.1:c.904C= ENSP00000490317.1:p.Arg302=
ENST00000636732.2:c.*621C= ENSP00000490175.1:n.*621C=
ENST00000636820.1:n.1004C=
ENST00000637045.1:c.568C= ENSP00000490141.1:p.Arg190=
ENST00000637267.2:c.904C= ENSP00000490293.2:p.Arg302=
ENST00000637304.1:c.568C= ENSP00000490872.1:p.Arg190=
ENST00000638007.1:c.568C= ENSP00000490723.1:p.Arg190=
ENST00000638087.1:c.568C= ENSP00000490673.1:p.Arg190=
ENST00000638128.1:c.127C= ENSP00000490934.1:p.Arg43=
ENST00000675069.1:c.-133-2361C= ENSP00000502467.1:n.-133-2361C=
ENST00000675145.1:n.1452C=
ENST00000689298.1:c.*753C= ENSP00000508434.1:n.*753C=
XM_006712881.2:c.904C= XP_006712944.1:p.Arg302=
XM_006712882.2:c.904C= XP_006712945.1:p.Arg302=
XM_011512231.1:c.895C= XP_011510533.1:p.Arg299=
XM_011512232.1:c.883C= XP_011510534.1:p.Arg295=