Canonical Allele Identifier: CA1294887203

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404021G= , CM000664.2:g.144404021G=	GRCh38
NC_000002.11:g.145161588G= , CM000664.1:g.145161588G=	GRCh37
NC_000002.10:g.144878058G=	NCBI36
NG_016431.1:g.121371C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*551C=	ENSP00000508434.1:n.*551C=
ENST00000440875.6:c.-76C=	ENSP00000475553.3:n.-76C=
ENST00000627532.3:c.702C= MANE Select	ENSP00000487174.1:p.His234=
ENST00000636026.2:c.702C=	ENSP00000490776.1:p.His234=
ENST00000636179.1:n.671C=
ENST00000636413.1:c.366C=	ENSP00000490508.1:p.His122=
ENST00000636471.1:c.702C=	ENSP00000490317.1:p.His234=
ENST00000636732.2:c.*419C=	ENSP00000490175.1:n.*419C=
ENST00000636820.1:n.802C=
ENST00000637045.1:c.366C=	ENSP00000490141.1:p.His122=
ENST00000637267.2:c.702C=	ENSP00000490293.2:p.His234=
ENST00000637304.1:c.366C=	ENSP00000490872.1:p.His122=
ENST00000638007.1:c.366C=	ENSP00000490723.1:p.His122=
ENST00000638087.1:c.366C=	ENSP00000490673.1:p.His122=
ENST00000638128.1:c.-76C=	ENSP00000490934.1:n.-76C=
ENST00000675069.1:c.-133-5171C=	ENSP00000502467.1:n.-133-5171C=
ENST00000303660.8:c.699C=	ENSP00000302501.4:p.His233=
ENST00000392861.6:c.786C=	ENSP00000376601.3:p.His262=
ENST00000409487.7:c.702C=	ENSP00000386854.2:p.His234=
ENST00000419938.5:c.441C=	ENSP00000394777.2:p.His147=
ENST00000427902.5:c.789C=	ENSP00000395496.2:p.His263=
ENST00000440875.5:c.687C=	ENSP00000475553.2:p.His229=
ENST00000497268.1:n.648C=
ENST00000539609.7:c.630C=	ENSP00000443792.2:p.His210=
ENST00000558170.6:c.702C=	ENSP00000454157.1:p.His234=
ENST00000627532.2:c.702C=	ENSP00000487174.1:p.His234=
NM_001171653.1:c.630C=	NP_001165124.1:p.His210=
NM_014795.3:c.702C=	NP_055610.1:p.His234=
XM_006712881.2:c.702C=	XP_006712944.1:p.His234=
XM_006712882.2:c.702C=	XP_006712945.1:p.His234=
XM_011512231.1:c.693C=	XP_011510533.1:p.His231=
XM_011512232.1:c.681C=	XP_011510534.1:p.His227=
NM_014795.4:c.702C= MANE Select	NP_055610.1:p.His234=
NM_001171653.2:c.630C=	NP_001165124.1:p.His210=