Canonical Allele Identifier: CA1294885268

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399352G= , CM000664.2:g.144399352G=	GRCh38
NC_000002.11:g.145156919G= , CM000664.1:g.145156919G=	GRCh37
NC_000002.10:g.144873389G=	NCBI36
NG_016431.1:g.126040C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1684C=	ENSP00000508434.1:n.*1684C=
ENST00000440875.6:c.1058C=	ENSP00000475553.3:p.Ala353=
ENST00000627532.3:c.1835C= MANE Select	ENSP00000487174.1:p.Ala612=
ENST00000636026.2:c.1835C=	ENSP00000490776.1:p.Ala612=
ENST00000636179.1:n.1804C=
ENST00000636413.1:c.1499C=	ENSP00000490508.1:p.Ala500=
ENST00000636471.1:c.1910C=	ENSP00000490317.1:p.Ala637=
ENST00000636732.2:c.*1552C=	ENSP00000490175.1:n.*1552C=
ENST00000636820.1:n.1935C=
ENST00000637045.1:c.1499C=	ENSP00000490141.1:p.Ala500=
ENST00000637267.2:c.1835C=	ENSP00000490293.2:p.Ala612=
ENST00000637304.1:c.1499C=	ENSP00000490872.1:p.Ala500=
ENST00000638007.1:c.1499C=	ENSP00000490723.1:p.Ala500=
ENST00000638087.1:c.1499C=	ENSP00000490673.1:p.Ala500=
ENST00000638128.1:c.1058C=	ENSP00000490934.1:p.Ala353=
ENST00000675069.1:c.-133-502C=	ENSP00000502467.1:n.-133-502C=
ENST00000675145.1:n.2383C=
ENST00000303660.8:c.1832C=	ENSP00000302501.4:p.Ala611=
ENST00000409487.7:c.1835C=	ENSP00000386854.2:p.Ala612=
ENST00000419938.5:c.655+1847C=	ENSP00000394777.2:n.655+1847C=
ENST00000427902.5:c.1922C=	ENSP00000395496.2:p.Ala641=
ENST00000440875.5:c.1167+185C=	ENSP00000475553.2:n.1167+185C=
ENST00000539609.7:c.1763C=	ENSP00000443792.2:p.Ala588=
ENST00000558170.6:c.1835C=	ENSP00000454157.1:p.Ala612=
ENST00000627532.2:c.1835C=	ENSP00000487174.1:p.Ala612=
NM_001171653.1:c.1763C=	NP_001165124.1:p.Ala588=
NM_014795.3:c.1835C=	NP_055610.1:p.Ala612=
XM_006712881.2:c.1835C=	XP_006712944.1:p.Ala612=
XM_006712882.2:c.1835C=	XP_006712945.1:p.Ala612=
XM_011512231.1:c.1826C=	XP_011510533.1:p.Ala609=
XM_011512232.1:c.1814C=	XP_011510534.1:p.Ala605=
NM_014795.4:c.1835C= MANE Select	NP_055610.1:p.Ala612=
NM_001171653.2:c.1763C=	NP_001165124.1:p.Ala588=