Canonical Allele Identifier: CA1294885996

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144401292G= , CM000664.2:g.144401292G=	GRCh38
NC_000002.11:g.145158859G= , CM000664.1:g.145158859G=	GRCh37
NC_000002.10:g.144875329G=	NCBI36
NG_016431.1:g.124100C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*672C=	ENSP00000508434.1:n.*672C=
ENST00000440875.6:c.46C=	ENSP00000475553.3:p.Gln16=
ENST00000627532.3:c.823C= MANE Select	ENSP00000487174.1:p.Gln275=
ENST00000636026.2:c.823C=	ENSP00000490776.1:p.Gln275=
ENST00000636179.1:n.792C=
ENST00000636413.1:c.487C=	ENSP00000490508.1:p.Gln163=
ENST00000636471.1:c.823C=	ENSP00000490317.1:p.Gln275=
ENST00000636732.2:c.*540C=	ENSP00000490175.1:n.*540C=
ENST00000636820.1:n.923C=
ENST00000637045.1:c.487C=	ENSP00000490141.1:p.Gln163=
ENST00000637267.2:c.823C=	ENSP00000490293.2:p.Gln275=
ENST00000637304.1:c.487C=	ENSP00000490872.1:p.Gln163=
ENST00000638007.1:c.487C=	ENSP00000490723.1:p.Gln163=
ENST00000638087.1:c.487C=	ENSP00000490673.1:p.Gln163=
ENST00000638128.1:c.46C=	ENSP00000490934.1:p.Gln16=
ENST00000675069.1:c.-133-2442C=	ENSP00000502467.1:n.-133-2442C=
ENST00000675145.1:n.1371C=
ENST00000303660.8:c.820C=	ENSP00000302501.4:p.Gln274=
ENST00000392861.6:c.907C=	ENSP00000376601.3:p.Gln303=
ENST00000409487.7:c.823C=	ENSP00000386854.2:p.Gln275=
ENST00000419938.5:c.562C=	ENSP00000394777.2:p.Gln188=
ENST00000427902.5:c.910C=	ENSP00000395496.2:p.Gln304=
ENST00000440875.5:c.808C=	ENSP00000475553.2:p.Gln270=
ENST00000539609.7:c.751C=	ENSP00000443792.2:p.Gln251=
ENST00000558170.6:c.823C=	ENSP00000454157.1:p.Gln275=
ENST00000627532.2:c.823C=	ENSP00000487174.1:p.Gln275=
NM_001171653.1:c.751C=	NP_001165124.1:p.Gln251=
NM_014795.3:c.823C=	NP_055610.1:p.Gln275=
XM_006712881.2:c.823C=	XP_006712944.1:p.Gln275=
XM_006712882.2:c.823C=	XP_006712945.1:p.Gln275=
XM_011512231.1:c.814C=	XP_011510533.1:p.Gln272=
XM_011512232.1:c.802C=	XP_011510534.1:p.Gln268=
NM_014795.4:c.823C= MANE Select	NP_055610.1:p.Gln275=
NM_001171653.2:c.751C=	NP_001165124.1:p.Gln251=