Canonical Allele Identifier: CA1294885007

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398716A= , CM000664.2:g.144398716A=	GRCh38
NC_000002.11:g.145156283A= , CM000664.1:g.145156283A=	GRCh37
NC_000002.10:g.144872753A=	NCBI36
NG_016431.1:g.126676T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2320T=	ENSP00000508434.1:n.*2320T=
ENST00000440875.6:c.1694T=	ENSP00000475553.3:p.Met565=
ENST00000627532.3:c.2471T= MANE Select	ENSP00000487174.1:p.Met824=
ENST00000636026.2:c.2471T=	ENSP00000490776.1:p.Met824=
ENST00000636179.1:n.2440T=
ENST00000636413.1:c.2135T=	ENSP00000490508.1:p.Met712=
ENST00000636471.1:c.2546T=	ENSP00000490317.1:p.Met849=
ENST00000636732.2:c.*2188T=	ENSP00000490175.1:n.*2188T=
ENST00000636820.1:n.2571T=
ENST00000637045.1:c.2135T=	ENSP00000490141.1:p.Met712=
ENST00000637304.1:c.2135T=	ENSP00000490872.1:p.Met712=
ENST00000638007.1:c.2135T=	ENSP00000490723.1:p.Met712=
ENST00000638087.1:c.2135T=	ENSP00000490673.1:p.Met712=
ENST00000638128.1:c.1694T=	ENSP00000490934.1:p.Met565=
ENST00000675069.1:c.2T=	ENSP00000502467.1:p.Met1=
ENST00000303660.8:c.2468T=	ENSP00000302501.4:p.Met823=
ENST00000409487.7:c.2471T=	ENSP00000386854.2:p.Met824=
ENST00000419938.5:c.655+2483T=	ENSP00000394777.2:n.655+2483T=
ENST00000440875.5:c.1168-788T=	ENSP00000475553.2:n.1168-788T=
ENST00000539609.7:c.2399T=	ENSP00000443792.2:p.Met800=
ENST00000558170.6:c.2471T=	ENSP00000454157.1:p.Met824=
ENST00000627532.2:c.2471T=	ENSP00000487174.1:p.Met824=
NM_001171653.1:c.2399T=	NP_001165124.1:p.Met800=
NM_014795.3:c.2471T=	NP_055610.1:p.Met824=
XM_006712881.2:c.2471T=	XP_006712944.1:p.Met824=
XM_006712882.2:c.2471T=	XP_006712945.1:p.Met824=
XM_011512231.1:c.2462T=	XP_011510533.1:p.Met821=
XM_011512232.1:c.2450T=	XP_011510534.1:p.Met817=
NM_014795.4:c.2471T= MANE Select	NP_055610.1:p.Met824=
NM_001171653.2:c.2399T=	NP_001165124.1:p.Met800=