Canonical Allele Identifier: CA1294884859

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398354T= , CM000664.2:g.144398354T=	GRCh38
NC_000002.11:g.145155921T= , CM000664.1:g.145155921T=	GRCh37
NC_000002.10:g.144872391T=	NCBI36
NG_016431.1:g.127038A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2682A=	ENSP00000508434.1:n.*2682A=
ENST00000440875.6:c.2056A=	ENSP00000475553.3:p.Thr686=
ENST00000627532.3:c.2833A= MANE Select	ENSP00000487174.1:p.Thr945=
ENST00000636026.2:c.2833A=	ENSP00000490776.1:p.Thr945=
ENST00000636179.1:n.2802A=
ENST00000636413.1:c.2497A=	ENSP00000490508.1:p.Thr833=
ENST00000636471.1:c.2908A=	ENSP00000490317.1:p.Thr970=
ENST00000636732.2:c.*2550A=	ENSP00000490175.1:n.*2550A=
ENST00000636820.1:n.2933A=
ENST00000637045.1:c.2497A=	ENSP00000490141.1:p.Thr833=
ENST00000637304.1:c.2497A=	ENSP00000490872.1:p.Thr833=
ENST00000638007.1:c.2497A=	ENSP00000490723.1:p.Thr833=
ENST00000638087.1:c.2497A=	ENSP00000490673.1:p.Thr833=
ENST00000638128.1:c.2056A=	ENSP00000490934.1:p.Thr686=
ENST00000675069.1:c.364A=	ENSP00000502467.1:p.Thr122=
ENST00000303660.8:c.2830A=	ENSP00000302501.4:p.Thr944=
ENST00000409487.7:c.2833A=	ENSP00000386854.2:p.Thr945=
ENST00000419938.5:c.655+2845A=	ENSP00000394777.2:n.655+2845A=
ENST00000440875.5:c.1168-426A=	ENSP00000475553.2:n.1168-426A=
ENST00000539609.7:c.2761A=	ENSP00000443792.2:p.Thr921=
ENST00000558170.6:c.2833A=	ENSP00000454157.1:p.Thr945=
ENST00000627532.2:c.2833A=	ENSP00000487174.1:p.Thr945=
NM_001171653.1:c.2761A=	NP_001165124.1:p.Thr921=
NM_014795.3:c.2833A=	NP_055610.1:p.Thr945=
XM_006712881.2:c.2833A=	XP_006712944.1:p.Thr945=
XM_006712882.2:c.2833A=	XP_006712945.1:p.Thr945=
XM_011512231.1:c.2824A=	XP_011510533.1:p.Thr942=
XM_011512232.1:c.2812A=	XP_011510534.1:p.Thr938=
NM_014795.4:c.2833A= MANE Select	NP_055610.1:p.Thr945=
NM_001171653.2:c.2761A=	NP_001165124.1:p.Thr921=