Canonical Allele Identifier: CA1294885029

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398797T= , CM000664.2:g.144398797T=	GRCh38
NC_000002.11:g.145156364T= , CM000664.1:g.145156364T=	GRCh37
NC_000002.10:g.144872834T=	NCBI36
NG_016431.1:g.126595A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2239A=	ENSP00000508434.1:n.*2239A=
ENST00000440875.6:c.1613A=	ENSP00000475553.3:p.His538=
ENST00000627532.3:c.2390A= MANE Select	ENSP00000487174.1:p.His797=
ENST00000636026.2:c.2390A=	ENSP00000490776.1:p.His797=
ENST00000636179.1:n.2359A=
ENST00000636413.1:c.2054A=	ENSP00000490508.1:p.His685=
ENST00000636471.1:c.2465A=	ENSP00000490317.1:p.His822=
ENST00000636732.2:c.*2107A=	ENSP00000490175.1:n.*2107A=
ENST00000636820.1:n.2490A=
ENST00000637045.1:c.2054A=	ENSP00000490141.1:p.His685=
ENST00000637304.1:c.2054A=	ENSP00000490872.1:p.His685=
ENST00000638007.1:c.2054A=	ENSP00000490723.1:p.His685=
ENST00000638087.1:c.2054A=	ENSP00000490673.1:p.His685=
ENST00000638128.1:c.1613A=	ENSP00000490934.1:p.His538=
ENST00000675069.1:c.-80A=	ENSP00000502467.1:n.-80A=
ENST00000675145.1:n.2938A=
ENST00000303660.8:c.2387A=	ENSP00000302501.4:p.His796=
ENST00000409487.7:c.2390A=	ENSP00000386854.2:p.His797=
ENST00000419938.5:c.655+2402A=	ENSP00000394777.2:n.655+2402A=
ENST00000440875.5:c.1167+740A=	ENSP00000475553.2:n.1167+740A=
ENST00000539609.7:c.2318A=	ENSP00000443792.2:p.His773=
ENST00000558170.6:c.2390A=	ENSP00000454157.1:p.His797=
ENST00000627532.2:c.2390A=	ENSP00000487174.1:p.His797=
NM_001171653.1:c.2318A=	NP_001165124.1:p.His773=
NM_014795.3:c.2390A=	NP_055610.1:p.His797=
XM_006712881.2:c.2390A=	XP_006712944.1:p.His797=
XM_006712882.2:c.2390A=	XP_006712945.1:p.His797=
XM_011512231.1:c.2381A=	XP_011510533.1:p.His794=
XM_011512232.1:c.2369A=	XP_011510534.1:p.His790=
NM_014795.4:c.2390A= MANE Select	NP_055610.1:p.His797=
NM_001171653.2:c.2318A=	NP_001165124.1:p.His773=