Canonical Allele Identifier: CA1294885038

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398816T= , CM000664.2:g.144398816T=	GRCh38
NC_000002.11:g.145156383T= , CM000664.1:g.145156383T=	GRCh37
NC_000002.10:g.144872853T=	NCBI36
NG_016431.1:g.126576A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2220A=	ENSP00000508434.1:n.*2220A=
ENST00000440875.6:c.1594A=	ENSP00000475553.3:p.Thr532=
ENST00000627532.3:c.2371A= MANE Select	ENSP00000487174.1:p.Thr791=
ENST00000636026.2:c.2371A=	ENSP00000490776.1:p.Thr791=
ENST00000636179.1:n.2340A=
ENST00000636413.1:c.2035A=	ENSP00000490508.1:p.Thr679=
ENST00000636471.1:c.2446A=	ENSP00000490317.1:p.Thr816=
ENST00000636732.2:c.*2088A=	ENSP00000490175.1:n.*2088A=
ENST00000636820.1:n.2471A=
ENST00000637045.1:c.2035A=	ENSP00000490141.1:p.Thr679=
ENST00000637304.1:c.2035A=	ENSP00000490872.1:p.Thr679=
ENST00000638007.1:c.2035A=	ENSP00000490723.1:p.Thr679=
ENST00000638087.1:c.2035A=	ENSP00000490673.1:p.Thr679=
ENST00000638128.1:c.1594A=	ENSP00000490934.1:p.Thr532=
ENST00000675069.1:c.-99A=	ENSP00000502467.1:n.-99A=
ENST00000675145.1:n.2919A=
ENST00000303660.8:c.2368A=	ENSP00000302501.4:p.Thr790=
ENST00000409487.7:c.2371A=	ENSP00000386854.2:p.Thr791=
ENST00000419938.5:c.655+2383A=	ENSP00000394777.2:n.655+2383A=
ENST00000440875.5:c.1167+721A=	ENSP00000475553.2:n.1167+721A=
ENST00000539609.7:c.2299A=	ENSP00000443792.2:p.Thr767=
ENST00000558170.6:c.2371A=	ENSP00000454157.1:p.Thr791=
ENST00000627532.2:c.2371A=	ENSP00000487174.1:p.Thr791=
NM_001171653.1:c.2299A=	NP_001165124.1:p.Thr767=
NM_014795.3:c.2371A=	NP_055610.1:p.Thr791=
XM_006712881.2:c.2371A=	XP_006712944.1:p.Thr791=
XM_006712882.2:c.2371A=	XP_006712945.1:p.Thr791=
XM_011512231.1:c.2362A=	XP_011510533.1:p.Thr788=
XM_011512232.1:c.2350A=	XP_011510534.1:p.Thr784=
NM_014795.4:c.2371A= MANE Select	NP_055610.1:p.Thr791=
NM_001171653.2:c.2299A=	NP_001165124.1:p.Thr767=