Canonical Allele Identifier: CA1294881368

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389855A= , CM000664.2:g.144389855A=	GRCh38
NC_000002.11:g.145147422A= , CM000664.1:g.145147422A=	GRCh37
NC_000002.10:g.144863892A=	NCBI36
NG_016431.1:g.135537T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3090T=	ENSP00000508434.1:n.*3090T=
ENST00000440875.6:c.2464T=	ENSP00000475553.3:p.Cys822=
ENST00000627532.3:c.3241T= MANE Select	ENSP00000487174.1:p.Cys1081=
ENST00000636026.2:c.3230+11T=	ENSP00000490776.1:n.3230+11T=
ENST00000636179.1:n.3210T=
ENST00000636413.1:c.2905T=	ENSP00000490508.1:p.Cys969=
ENST00000636471.1:c.3316T=	ENSP00000490317.1:p.Cys1106=
ENST00000636732.2:c.*2958T=	ENSP00000490175.1:n.*2958T=
ENST00000636820.1:n.3341T=
ENST00000637045.1:c.2905T=	ENSP00000490141.1:p.Cys969=
ENST00000637304.1:c.2905T=	ENSP00000490872.1:p.Cys969=
ENST00000638007.1:c.2905T=	ENSP00000490723.1:p.Cys969=
ENST00000638087.1:c.2905T=	ENSP00000490673.1:p.Cys969=
ENST00000638128.1:c.2464T=	ENSP00000490934.1:p.Cys822=
ENST00000639389.1:c.151+6557T=	ENSP00000492572.1:n.151+6557T=
ENST00000647488.1:c.461T=	ENSP00000494820.1:n.461T=
ENST00000675069.1:c.772T=	ENSP00000502467.1:p.Cys258=
ENST00000303660.8:c.3238T=	ENSP00000302501.4:p.Cys1080=
ENST00000409487.7:c.3241T=	ENSP00000386854.2:p.Cys1081=
ENST00000419938.5:c.656-973T=	ENSP00000394777.2:n.656-973T=
ENST00000539609.7:c.3169T=	ENSP00000443792.2:p.Cys1057=
ENST00000558170.6:c.3241T=	ENSP00000454157.1:p.Cys1081=
ENST00000627532.2:c.3241T=	ENSP00000487174.1:p.Cys1081=
NM_001171653.1:c.3169T=	NP_001165124.1:p.Cys1057=
NM_014795.3:c.3241T=	NP_055610.1:p.Cys1081=
XM_006712881.2:c.3241T=	XP_006712944.1:p.Cys1081=
XM_006712882.2:c.3241T=	XP_006712945.1:p.Cys1081=
XM_011512231.1:c.3232T=	XP_011510533.1:p.Cys1078=
XM_011512232.1:c.3220T=	XP_011510534.1:p.Cys1074=
NM_014795.4:c.3241T= MANE Select	NP_055610.1:p.Cys1081=
NM_001171653.2:c.3169T=	NP_001165124.1:p.Cys1057=