Canonical Allele Identifier: CA1294887184

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403977G= , CM000664.2:g.144403977G=	GRCh38
NC_000002.11:g.145161544G= , CM000664.1:g.145161544G=	GRCh37
NC_000002.10:g.144878014G=	NCBI36
NG_016431.1:g.121415C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*595C=	ENSP00000508434.1:n.*595C=
ENST00000440875.6:c.-32C=	ENSP00000475553.3:n.-32C=
ENST00000627532.3:c.746C= MANE Select	ENSP00000487174.1:p.Thr249=
ENST00000636026.2:c.746C=	ENSP00000490776.1:p.Thr249=
ENST00000636179.1:n.715C=
ENST00000636413.1:c.410C=	ENSP00000490508.1:p.Thr137=
ENST00000636471.1:c.746C=	ENSP00000490317.1:p.Thr249=
ENST00000636732.2:c.*463C=	ENSP00000490175.1:n.*463C=
ENST00000636820.1:n.846C=
ENST00000637045.1:c.410C=	ENSP00000490141.1:p.Thr137=
ENST00000637267.2:c.746C=	ENSP00000490293.2:p.Thr249=
ENST00000637304.1:c.410C=	ENSP00000490872.1:p.Thr137=
ENST00000638007.1:c.410C=	ENSP00000490723.1:p.Thr137=
ENST00000638087.1:c.410C=	ENSP00000490673.1:p.Thr137=
ENST00000638128.1:c.-32C=	ENSP00000490934.1:n.-32C=
ENST00000675069.1:c.-133-5127C=	ENSP00000502467.1:n.-133-5127C=
ENST00000303660.8:c.743C=	ENSP00000302501.4:p.Thr248=
ENST00000392861.6:c.830C=	ENSP00000376601.3:p.Thr277=
ENST00000409487.7:c.746C=	ENSP00000386854.2:p.Thr249=
ENST00000419938.5:c.485C=	ENSP00000394777.2:p.Thr162=
ENST00000427902.5:c.833C=	ENSP00000395496.2:p.Thr278=
ENST00000440875.5:c.731C=	ENSP00000475553.2:p.Thr244=
ENST00000539609.7:c.674C=	ENSP00000443792.2:p.Thr225=
ENST00000558170.6:c.746C=	ENSP00000454157.1:p.Thr249=
ENST00000627532.2:c.746C=	ENSP00000487174.1:p.Thr249=
NM_001171653.1:c.674C=	NP_001165124.1:p.Thr225=
NM_014795.3:c.746C=	NP_055610.1:p.Thr249=
XM_006712881.2:c.746C=	XP_006712944.1:p.Thr249=
XM_006712882.2:c.746C=	XP_006712945.1:p.Thr249=
XM_011512231.1:c.737C=	XP_011510533.1:p.Thr246=
XM_011512232.1:c.725C=	XP_011510534.1:p.Thr242=
NM_014795.4:c.746C= MANE Select	NP_055610.1:p.Thr249=
NM_001171653.2:c.674C=	NP_001165124.1:p.Thr225=