Canonical Allele Identifier: CA1294885028

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398793A= , CM000664.2:g.144398793A=	GRCh38
NC_000002.11:g.145156360A= , CM000664.1:g.145156360A=	GRCh37
NC_000002.10:g.144872830A=	NCBI36
NG_016431.1:g.126599T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2243T=	ENSP00000508434.1:n.*2243T=
ENST00000440875.6:c.1617T=	ENSP00000475553.3:p.Ser539=
ENST00000627532.3:c.2394T= MANE Select	ENSP00000487174.1:p.Ser798=
ENST00000636026.2:c.2394T=	ENSP00000490776.1:p.Ser798=
ENST00000636179.1:n.2363T=
ENST00000636413.1:c.2058T=	ENSP00000490508.1:p.Ser686=
ENST00000636471.1:c.2469T=	ENSP00000490317.1:p.Ser823=
ENST00000636732.2:c.*2111T=	ENSP00000490175.1:n.*2111T=
ENST00000636820.1:n.2494T=
ENST00000637045.1:c.2058T=	ENSP00000490141.1:p.Ser686=
ENST00000637304.1:c.2058T=	ENSP00000490872.1:p.Ser686=
ENST00000638007.1:c.2058T=	ENSP00000490723.1:p.Ser686=
ENST00000638087.1:c.2058T=	ENSP00000490673.1:p.Ser686=
ENST00000638128.1:c.1617T=	ENSP00000490934.1:p.Ser539=
ENST00000675069.1:c.-76T=	ENSP00000502467.1:n.-76T=
ENST00000675145.1:n.2942T=
ENST00000303660.8:c.2391T=	ENSP00000302501.4:p.Ser797=
ENST00000409487.7:c.2394T=	ENSP00000386854.2:p.Ser798=
ENST00000419938.5:c.655+2406T=	ENSP00000394777.2:n.655+2406T=
ENST00000440875.5:c.1167+744T=	ENSP00000475553.2:n.1167+744T=
ENST00000539609.7:c.2322T=	ENSP00000443792.2:p.Ser774=
ENST00000558170.6:c.2394T=	ENSP00000454157.1:p.Ser798=
ENST00000627532.2:c.2394T=	ENSP00000487174.1:p.Ser798=
NM_001171653.1:c.2322T=	NP_001165124.1:p.Ser774=
NM_014795.3:c.2394T=	NP_055610.1:p.Ser798=
XM_006712881.2:c.2394T=	XP_006712944.1:p.Ser798=
XM_006712882.2:c.2394T=	XP_006712945.1:p.Ser798=
XM_011512231.1:c.2385T=	XP_011510533.1:p.Ser795=
XM_011512232.1:c.2373T=	XP_011510534.1:p.Ser791=
NM_014795.4:c.2394T= MANE Select	NP_055610.1:p.Ser798=
NM_001171653.2:c.2322T=	NP_001165124.1:p.Ser774=