Canonical Allele Identifier: CA1294887217

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404063G= , CM000664.2:g.144404063G=	GRCh38
NC_000002.11:g.145161630G= , CM000664.1:g.145161630G=	GRCh37
NC_000002.10:g.144878100G=	NCBI36
NG_016431.1:g.121329C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*509C=	ENSP00000508434.1:n.*509C=
ENST00000440875.6:c.-118C=	ENSP00000475553.3:n.-118C=
ENST00000627532.3:c.660C= MANE Select	ENSP00000487174.1:p.Tyr220=
ENST00000636026.2:c.660C=	ENSP00000490776.1:p.Tyr220=
ENST00000636179.1:n.629C=
ENST00000636413.1:c.324C=	ENSP00000490508.1:p.Tyr108=
ENST00000636471.1:c.660C=	ENSP00000490317.1:p.Tyr220=
ENST00000636732.2:c.*377C=	ENSP00000490175.1:n.*377C=
ENST00000636820.1:n.760C=
ENST00000637045.1:c.324C=	ENSP00000490141.1:p.Tyr108=
ENST00000637267.2:c.660C=	ENSP00000490293.2:p.Tyr220=
ENST00000637304.1:c.324C=	ENSP00000490872.1:p.Tyr108=
ENST00000638007.1:c.324C=	ENSP00000490723.1:p.Tyr108=
ENST00000638087.1:c.324C=	ENSP00000490673.1:p.Tyr108=
ENST00000638128.1:c.-118C=	ENSP00000490934.1:n.-118C=
ENST00000675069.1:c.-133-5213C=	ENSP00000502467.1:n.-133-5213C=
ENST00000303660.8:c.657C=	ENSP00000302501.4:p.Tyr219=
ENST00000392861.6:c.744C=	ENSP00000376601.3:p.Tyr248=
ENST00000409487.7:c.660C=	ENSP00000386854.2:p.Tyr220=
ENST00000419938.5:c.399C=	ENSP00000394777.2:p.Tyr133=
ENST00000427902.5:c.747C=	ENSP00000395496.2:p.Tyr249=
ENST00000440875.5:c.645C=	ENSP00000475553.2:p.Tyr215=
ENST00000497268.1:n.606C=
ENST00000539609.7:c.588C=	ENSP00000443792.2:p.Tyr196=
ENST00000558170.6:c.660C=	ENSP00000454157.1:p.Tyr220=
ENST00000627532.2:c.660C=	ENSP00000487174.1:p.Tyr220=
NM_001171653.1:c.588C=	NP_001165124.1:p.Tyr196=
NM_014795.3:c.660C=	NP_055610.1:p.Tyr220=
XM_006712881.2:c.660C=	XP_006712944.1:p.Tyr220=
XM_006712882.2:c.660C=	XP_006712945.1:p.Tyr220=
XM_011512231.1:c.651C=	XP_011510533.1:p.Tyr217=
XM_011512232.1:c.639C=	XP_011510534.1:p.Tyr213=
NM_014795.4:c.660C= MANE Select	NP_055610.1:p.Tyr220=
NM_001171653.2:c.588C=	NP_001165124.1:p.Tyr196=