Canonical Allele Identifier: CA1294885015

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398751C= , CM000664.2:g.144398751C=	GRCh38
NC_000002.11:g.145156318C= , CM000664.1:g.145156318C=	GRCh37
NC_000002.10:g.144872788C=	NCBI36
NG_016431.1:g.126641G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2285G=	ENSP00000508434.1:n.*2285G=
ENST00000440875.6:c.1659G=	ENSP00000475553.3:p.Gln553=
ENST00000627532.3:c.2436G= MANE Select	ENSP00000487174.1:p.Gln812=
ENST00000636026.2:c.2436G=	ENSP00000490776.1:p.Gln812=
ENST00000636179.1:n.2405G=
ENST00000636413.1:c.2100G=	ENSP00000490508.1:p.Gln700=
ENST00000636471.1:c.2511G=	ENSP00000490317.1:p.Gln837=
ENST00000636732.2:c.*2153G=	ENSP00000490175.1:n.*2153G=
ENST00000636820.1:n.2536G=
ENST00000637045.1:c.2100G=	ENSP00000490141.1:p.Gln700=
ENST00000637304.1:c.2100G=	ENSP00000490872.1:p.Gln700=
ENST00000638007.1:c.2100G=	ENSP00000490723.1:p.Gln700=
ENST00000638087.1:c.2100G=	ENSP00000490673.1:p.Gln700=
ENST00000638128.1:c.1659G=	ENSP00000490934.1:p.Gln553=
ENST00000675069.1:c.-34G=	ENSP00000502467.1:n.-34G=
ENST00000675145.1:n.2984G=
ENST00000303660.8:c.2433G=	ENSP00000302501.4:p.Gln811=
ENST00000409487.7:c.2436G=	ENSP00000386854.2:p.Gln812=
ENST00000419938.5:c.655+2448G=	ENSP00000394777.2:n.655+2448G=
ENST00000440875.5:c.1167+786G=	ENSP00000475553.2:n.1167+786G=
ENST00000539609.7:c.2364G=	ENSP00000443792.2:p.Gln788=
ENST00000558170.6:c.2436G=	ENSP00000454157.1:p.Gln812=
ENST00000627532.2:c.2436G=	ENSP00000487174.1:p.Gln812=
NM_001171653.1:c.2364G=	NP_001165124.1:p.Gln788=
NM_014795.3:c.2436G=	NP_055610.1:p.Gln812=
XM_006712881.2:c.2436G=	XP_006712944.1:p.Gln812=
XM_006712882.2:c.2436G=	XP_006712945.1:p.Gln812=
XM_011512231.1:c.2427G=	XP_011510533.1:p.Gln809=
XM_011512232.1:c.2415G=	XP_011510534.1:p.Gln805=
NM_014795.4:c.2436G= MANE Select	NP_055610.1:p.Gln812=
NM_001171653.2:c.2364G=	NP_001165124.1:p.Gln788=