Canonical Allele Identifier: CA1294885277

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399385C= , CM000664.2:g.144399385C=	GRCh38
NC_000002.11:g.145156952C= , CM000664.1:g.145156952C=	GRCh37
NC_000002.10:g.144873422C=	NCBI36
NG_016431.1:g.126007G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1651G=	ENSP00000508434.1:n.*1651G=
ENST00000440875.6:c.1025G=	ENSP00000475553.3:p.Arg342=
ENST00000627532.3:c.1802G= MANE Select	ENSP00000487174.1:p.Arg601=
ENST00000636026.2:c.1802G=	ENSP00000490776.1:p.Arg601=
ENST00000636179.1:n.1771G=
ENST00000636413.1:c.1466G=	ENSP00000490508.1:p.Arg489=
ENST00000636471.1:c.1877G=	ENSP00000490317.1:p.Arg626=
ENST00000636732.2:c.*1519G=	ENSP00000490175.1:n.*1519G=
ENST00000636820.1:n.1902G=
ENST00000637045.1:c.1466G=	ENSP00000490141.1:p.Arg489=
ENST00000637267.2:c.1802G=	ENSP00000490293.2:p.Arg601=
ENST00000637304.1:c.1466G=	ENSP00000490872.1:p.Arg489=
ENST00000638007.1:c.1466G=	ENSP00000490723.1:p.Arg489=
ENST00000638087.1:c.1466G=	ENSP00000490673.1:p.Arg489=
ENST00000638128.1:c.1025G=	ENSP00000490934.1:p.Arg342=
ENST00000675069.1:c.-133-535G=	ENSP00000502467.1:n.-133-535G=
ENST00000675145.1:n.2350G=
ENST00000303660.8:c.1799G=	ENSP00000302501.4:p.Arg600=
ENST00000409487.7:c.1802G=	ENSP00000386854.2:p.Arg601=
ENST00000419938.5:c.655+1814G=	ENSP00000394777.2:n.655+1814G=
ENST00000427902.5:c.1889G=	ENSP00000395496.2:p.Arg630=
ENST00000440875.5:c.1167+152G=	ENSP00000475553.2:n.1167+152G=
ENST00000539609.7:c.1730G=	ENSP00000443792.2:p.Arg577=
ENST00000558170.6:c.1802G=	ENSP00000454157.1:p.Arg601=
ENST00000627532.2:c.1802G=	ENSP00000487174.1:p.Arg601=
NM_001171653.1:c.1730G=	NP_001165124.1:p.Arg577=
NM_014795.3:c.1802G=	NP_055610.1:p.Arg601=
XM_006712881.2:c.1802G=	XP_006712944.1:p.Arg601=
XM_006712882.2:c.1802G=	XP_006712945.1:p.Arg601=
XM_011512231.1:c.1793G=	XP_011510533.1:p.Arg598=
XM_011512232.1:c.1781G=	XP_011510534.1:p.Arg594=
NM_014795.4:c.1802G= MANE Select	NP_055610.1:p.Arg601=
NM_001171653.2:c.1730G=	NP_001165124.1:p.Arg577=