Canonical Allele Identifier: CA1294881294

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389673C= , CM000664.2:g.144389673C=	GRCh38
NC_000002.11:g.145147240C= , CM000664.1:g.145147240C=	GRCh37
NC_000002.10:g.144863710C=	NCBI36
NG_016431.1:g.135719G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3272G=	ENSP00000508434.1:n.*3272G=
ENST00000440875.6:c.2646G=	ENSP00000475553.3:p.Glu882=
ENST00000627532.3:c.3423G= MANE Select	ENSP00000487174.1:p.Glu1141=
ENST00000636026.2:c.3311G=	ENSP00000490776.1:p.Arg1104=
ENST00000636179.1:n.3392G=
ENST00000636413.1:c.3087G=	ENSP00000490508.1:p.Glu1029=
ENST00000636471.1:c.3498G=	ENSP00000490317.1:p.Glu1166=
ENST00000636732.2:c.*3140G=	ENSP00000490175.1:n.*3140G=
ENST00000636820.1:n.3523G=
ENST00000637045.1:c.3087G=	ENSP00000490141.1:p.Glu1029=
ENST00000637304.1:c.3087G=	ENSP00000490872.1:p.Glu1029=
ENST00000638007.1:c.3087G=	ENSP00000490723.1:p.Glu1029=
ENST00000638087.1:c.3087G=	ENSP00000490673.1:p.Glu1029=
ENST00000638128.1:c.2646G=	ENSP00000490934.1:p.Glu882=
ENST00000639389.1:c.151+6739G=	ENSP00000492572.1:n.151+6739G=
ENST00000647488.1:c.643G=	ENSP00000494820.1:n.643G=
ENST00000675069.1:c.954G=	ENSP00000502467.1:p.Glu318=
ENST00000303660.8:c.3420G=	ENSP00000302501.4:p.Glu1140=
ENST00000409487.7:c.3423G=	ENSP00000386854.2:p.Glu1141=
ENST00000419938.5:c.656-791G=	ENSP00000394777.2:n.656-791G=
ENST00000539609.7:c.3351G=	ENSP00000443792.2:p.Glu1117=
ENST00000558170.6:c.3423G=	ENSP00000454157.1:p.Glu1141=
ENST00000627532.2:c.3423G=	ENSP00000487174.1:p.Glu1141=
NM_001171653.1:c.3351G=	NP_001165124.1:p.Glu1117=
NM_014795.3:c.3423G=	NP_055610.1:p.Glu1141=
XM_006712881.2:c.3423G=	XP_006712944.1:p.Glu1141=
XM_006712882.2:c.3423G=	XP_006712945.1:p.Glu1141=
XM_011512231.1:c.3414G=	XP_011510533.1:p.Glu1138=
XM_011512232.1:c.3402G=	XP_011510534.1:p.Glu1134=
NM_014795.4:c.3423G= MANE Select	NP_055610.1:p.Glu1141=
NM_001171653.2:c.3351G=	NP_001165124.1:p.Glu1117=