Canonical Allele Identifier: CA1294884928

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398530A= , CM000664.2:g.144398530A=	GRCh38
NC_000002.11:g.145156097A= , CM000664.1:g.145156097A=	GRCh37
NC_000002.10:g.144872567A=	NCBI36
NG_016431.1:g.126862T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2506T=	ENSP00000508434.1:n.*2506T=
ENST00000440875.6:c.1880T=	ENSP00000475553.3:p.Met627=
ENST00000627532.3:c.2657T= MANE Select	ENSP00000487174.1:p.Met886=
ENST00000636026.2:c.2657T=	ENSP00000490776.1:p.Met886=
ENST00000636179.1:n.2626T=
ENST00000636413.1:c.2321T=	ENSP00000490508.1:p.Met774=
ENST00000636471.1:c.2732T=	ENSP00000490317.1:p.Met911=
ENST00000636732.2:c.*2374T=	ENSP00000490175.1:n.*2374T=
ENST00000636820.1:n.2757T=
ENST00000637045.1:c.2321T=	ENSP00000490141.1:p.Met774=
ENST00000637304.1:c.2321T=	ENSP00000490872.1:p.Met774=
ENST00000638007.1:c.2321T=	ENSP00000490723.1:p.Met774=
ENST00000638087.1:c.2321T=	ENSP00000490673.1:p.Met774=
ENST00000638128.1:c.1880T=	ENSP00000490934.1:p.Met627=
ENST00000675069.1:c.188T=	ENSP00000502467.1:p.Met63=
ENST00000303660.8:c.2654T=	ENSP00000302501.4:p.Met885=
ENST00000409487.7:c.2657T=	ENSP00000386854.2:p.Met886=
ENST00000419938.5:c.655+2669T=	ENSP00000394777.2:n.655+2669T=
ENST00000440875.5:c.1168-602T=	ENSP00000475553.2:n.1168-602T=
ENST00000539609.7:c.2585T=	ENSP00000443792.2:p.Met862=
ENST00000558170.6:c.2657T=	ENSP00000454157.1:p.Met886=
ENST00000627532.2:c.2657T=	ENSP00000487174.1:p.Met886=
NM_001171653.1:c.2585T=	NP_001165124.1:p.Met862=
NM_014795.3:c.2657T=	NP_055610.1:p.Met886=
XM_006712881.2:c.2657T=	XP_006712944.1:p.Met886=
XM_006712882.2:c.2657T=	XP_006712945.1:p.Met886=
XM_011512231.1:c.2648T=	XP_011510533.1:p.Met883=
XM_011512232.1:c.2636T=	XP_011510534.1:p.Met879=
NM_014795.4:c.2657T= MANE Select	NP_055610.1:p.Met886=
NM_001171653.2:c.2585T=	NP_001165124.1:p.Met862=