Canonical Allele Identifier: CA1294885402

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399748G= , CM000664.2:g.144399748G=	GRCh38
NC_000002.11:g.145157315G= , CM000664.1:g.145157315G=	GRCh37
NC_000002.10:g.144873785G=	NCBI36
NG_016431.1:g.125644C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1288C=	ENSP00000508434.1:n.*1288C=
ENST00000440875.6:c.662C=	ENSP00000475553.3:p.Ala221=
ENST00000627532.3:c.1439C= MANE Select	ENSP00000487174.1:p.Ala480=
ENST00000636026.2:c.1439C=	ENSP00000490776.1:p.Ala480=
ENST00000636179.1:n.1408C=
ENST00000636413.1:c.1103C=	ENSP00000490508.1:p.Ala368=
ENST00000636471.1:c.1514C=	ENSP00000490317.1:p.Ala505=
ENST00000636732.2:c.*1156C=	ENSP00000490175.1:n.*1156C=
ENST00000636820.1:n.1539C=
ENST00000637045.1:c.1103C=	ENSP00000490141.1:p.Ala368=
ENST00000637267.2:c.1439C=	ENSP00000490293.2:p.Ala480=
ENST00000637304.1:c.1103C=	ENSP00000490872.1:p.Ala368=
ENST00000638007.1:c.1103C=	ENSP00000490723.1:p.Ala368=
ENST00000638087.1:c.1103C=	ENSP00000490673.1:p.Ala368=
ENST00000638128.1:c.662C=	ENSP00000490934.1:p.Ala221=
ENST00000675069.1:c.-133-898C=	ENSP00000502467.1:n.-133-898C=
ENST00000675145.1:n.1987C=
ENST00000303660.8:c.1436C=	ENSP00000302501.4:p.Ala479=
ENST00000409487.7:c.1439C=	ENSP00000386854.2:p.Ala480=
ENST00000419938.5:c.655+1451C=	ENSP00000394777.2:n.655+1451C=
ENST00000427902.5:c.1526C=	ENSP00000395496.2:p.Ala509=
ENST00000440875.5:c.1154-198C=	ENSP00000475553.2:n.1154-198C=
ENST00000539609.7:c.1367C=	ENSP00000443792.2:p.Ala456=
ENST00000558170.6:c.1439C=	ENSP00000454157.1:p.Ala480=
ENST00000627532.2:c.1439C=	ENSP00000487174.1:p.Ala480=
NM_001171653.1:c.1367C=	NP_001165124.1:p.Ala456=
NM_014795.3:c.1439C=	NP_055610.1:p.Ala480=
XM_006712881.2:c.1439C=	XP_006712944.1:p.Ala480=
XM_006712882.2:c.1439C=	XP_006712945.1:p.Ala480=
XM_011512231.1:c.1430C=	XP_011510533.1:p.Ala477=
XM_011512232.1:c.1418C=	XP_011510534.1:p.Ala473=
NM_014795.4:c.1439C= MANE Select	NP_055610.1:p.Ala480=
NM_001171653.2:c.1367C=	NP_001165124.1:p.Ala456=