Canonical Allele Identifier: CA1294887221

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404072G= , CM000664.2:g.144404072G=	GRCh38
NC_000002.11:g.145161639G= , CM000664.1:g.145161639G=	GRCh37
NC_000002.10:g.144878109G=	NCBI36
NG_016431.1:g.121320C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*500C=	ENSP00000508434.1:n.*500C=
ENST00000440875.6:c.-127C=	ENSP00000475553.3:n.-127C=
ENST00000627532.3:c.651C= MANE Select	ENSP00000487174.1:p.Asp217=
ENST00000636026.2:c.651C=	ENSP00000490776.1:p.Asp217=
ENST00000636179.1:n.620C=
ENST00000636413.1:c.315C=	ENSP00000490508.1:p.Asp105=
ENST00000636471.1:c.651C=	ENSP00000490317.1:p.Asp217=
ENST00000636732.2:c.*368C=	ENSP00000490175.1:n.*368C=
ENST00000636820.1:n.751C=
ENST00000637045.1:c.315C=	ENSP00000490141.1:p.Asp105=
ENST00000637267.2:c.651C=	ENSP00000490293.2:p.Asp217=
ENST00000637304.1:c.315C=	ENSP00000490872.1:p.Asp105=
ENST00000638007.1:c.315C=	ENSP00000490723.1:p.Asp105=
ENST00000638087.1:c.315C=	ENSP00000490673.1:p.Asp105=
ENST00000638128.1:c.-127C=	ENSP00000490934.1:n.-127C=
ENST00000675069.1:c.-133-5222C=	ENSP00000502467.1:n.-133-5222C=
ENST00000303660.8:c.648C=	ENSP00000302501.4:p.Asp216=
ENST00000392861.6:c.735C=	ENSP00000376601.3:p.Asp245=
ENST00000409487.7:c.651C=	ENSP00000386854.2:p.Asp217=
ENST00000419938.5:c.390C=	ENSP00000394777.2:p.Asp130=
ENST00000427902.5:c.738C=	ENSP00000395496.2:p.Asp246=
ENST00000440875.5:c.636C=	ENSP00000475553.2:p.Asp212=
ENST00000497268.1:n.597C=
ENST00000539609.7:c.579C=	ENSP00000443792.2:p.Asp193=
ENST00000558170.6:c.651C=	ENSP00000454157.1:p.Asp217=
ENST00000627532.2:c.651C=	ENSP00000487174.1:p.Asp217=
NM_001171653.1:c.579C=	NP_001165124.1:p.Asp193=
NM_014795.3:c.651C=	NP_055610.1:p.Asp217=
XM_006712881.2:c.651C=	XP_006712944.1:p.Asp217=
XM_006712882.2:c.651C=	XP_006712945.1:p.Asp217=
XM_011512231.1:c.642C=	XP_011510533.1:p.Asp214=
XM_011512232.1:c.630C=	XP_011510534.1:p.Asp210=
NM_014795.4:c.651C= MANE Select	NP_055610.1:p.Asp217=
NM_001171653.2:c.579C=	NP_001165124.1:p.Asp193=