Canonical Allele Identifier: CA1294898488

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144429820C= , CM000664.2:g.144429820C=	GRCh38
NC_000002.11:g.145187387C= , CM000664.1:g.145187387C=	GRCh37
NC_000002.10:g.144903857C=	NCBI36
NG_016431.1:g.95572G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000637591.2:n.429G=
ENST00000689298.1:c.*201G=	ENSP00000508434.1:n.*201G=
ENST00000440875.6:c.-426G=	ENSP00000475553.3:n.-426G=
ENST00000627532.3:c.280G= MANE Select	ENSP00000487174.1:p.Glu94=
ENST00000636026.2:c.280G=	ENSP00000490776.1:p.Glu94=
ENST00000636179.1:n.249G=
ENST00000636413.1:c.-57G=	ENSP00000490508.1:n.-57G=
ENST00000636471.1:c.280G=	ENSP00000490317.1:p.Glu94=
ENST00000636732.2:c.280G=	ENSP00000490175.1:p.Glu94=
ENST00000636820.1:n.380G=
ENST00000637045.1:c.-57G=	ENSP00000490141.1:n.-57G=
ENST00000637267.2:c.280G=	ENSP00000490293.2:p.Glu94=
ENST00000637304.1:c.-57G=	ENSP00000490872.1:n.-57G=
ENST00000638007.1:c.-57G=	ENSP00000490723.1:n.-57G=
ENST00000638087.1:c.-57G=	ENSP00000490673.1:n.-57G=
ENST00000638128.1:c.-426G=	ENSP00000490934.1:n.-426G=
ENST00000675069.1:c.-133-30970G=	ENSP00000502467.1:n.-133-30970G=
ENST00000303660.8:c.280G=	ENSP00000302501.4:p.Glu94=
ENST00000392861.6:c.364G=	ENSP00000376601.3:p.Glu122=
ENST00000409211.5:c.280G=	ENSP00000387256.2:p.Glu94=
ENST00000409487.7:c.280G=	ENSP00000386854.2:p.Glu94=
ENST00000419938.5:c.280G=	ENSP00000394777.2:p.Glu94=
ENST00000427902.5:c.367G=	ENSP00000395496.2:p.Glu123=
ENST00000431672.4:c.280G=	ENSP00000475267.2:p.Glu94=
ENST00000434448.5:c.*211G=	ENSP00000487261.1:n.*211G=
ENST00000440875.5:c.265G=	ENSP00000475553.2:p.Glu89=
ENST00000461784.3:n.487G=
ENST00000465308.5:c.280G=	ENSP00000487476.1:p.Glu94=
ENST00000472146.5:n.530G=
ENST00000476394.5:n.384G=
ENST00000479735.1:n.511G=
ENST00000539609.7:c.280G=	ENSP00000443792.2:p.Glu94=
ENST00000558170.6:c.280G=	ENSP00000454157.1:p.Glu94=
ENST00000627532.2:c.280G=	ENSP00000487174.1:p.Glu94=
ENST00000627856.2:n.240G=
NM_001171653.1:c.280G=	NP_001165124.1:p.Glu94=
NM_014795.3:c.280G=	NP_055610.1:p.Glu94=
XM_006712881.2:c.280G=	XP_006712944.1:p.Glu94=
XM_006712882.2:c.280G=	XP_006712945.1:p.Glu94=
XM_011512231.1:c.271G=	XP_011510533.1:p.Glu91=
XM_011512232.1:c.259G=	XP_011510534.1:p.Glu87=
NM_014795.4:c.280G= MANE Select	NP_055610.1:p.Glu94=
NM_001171653.2:c.280G=	NP_001165124.1:p.Glu94=