Canonical Allele Identifier: CA1294885398

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399738A= , CM000664.2:g.144399738A=	GRCh38
NC_000002.11:g.145157305A= , CM000664.1:g.145157305A=	GRCh37
NC_000002.10:g.144873775A=	NCBI36
NG_016431.1:g.125654T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1298T=	ENSP00000508434.1:n.*1298T=
ENST00000440875.6:c.672T=	ENSP00000475553.3:p.Ile224=
ENST00000627532.3:c.1449T= MANE Select	ENSP00000487174.1:p.Ile483=
ENST00000636026.2:c.1449T=	ENSP00000490776.1:p.Ile483=
ENST00000636179.1:n.1418T=
ENST00000636413.1:c.1113T=	ENSP00000490508.1:p.Ile371=
ENST00000636471.1:c.1524T=	ENSP00000490317.1:p.Ile508=
ENST00000636732.2:c.*1166T=	ENSP00000490175.1:n.*1166T=
ENST00000636820.1:n.1549T=
ENST00000637045.1:c.1113T=	ENSP00000490141.1:p.Ile371=
ENST00000637267.2:c.1449T=	ENSP00000490293.2:p.Ile483=
ENST00000637304.1:c.1113T=	ENSP00000490872.1:p.Ile371=
ENST00000638007.1:c.1113T=	ENSP00000490723.1:p.Ile371=
ENST00000638087.1:c.1113T=	ENSP00000490673.1:p.Ile371=
ENST00000638128.1:c.672T=	ENSP00000490934.1:p.Ile224=
ENST00000675069.1:c.-133-888T=	ENSP00000502467.1:n.-133-888T=
ENST00000675145.1:n.1997T=
ENST00000303660.8:c.1446T=	ENSP00000302501.4:p.Ile482=
ENST00000409487.7:c.1449T=	ENSP00000386854.2:p.Ile483=
ENST00000419938.5:c.655+1461T=	ENSP00000394777.2:n.655+1461T=
ENST00000427902.5:c.1536T=	ENSP00000395496.2:p.Ile512=
ENST00000440875.5:c.1154-188T=	ENSP00000475553.2:n.1154-188T=
ENST00000539609.7:c.1377T=	ENSP00000443792.2:p.Ile459=
ENST00000558170.6:c.1449T=	ENSP00000454157.1:p.Ile483=
ENST00000627532.2:c.1449T=	ENSP00000487174.1:p.Ile483=
NM_001171653.1:c.1377T=	NP_001165124.1:p.Ile459=
NM_014795.3:c.1449T=	NP_055610.1:p.Ile483=
XM_006712881.2:c.1449T=	XP_006712944.1:p.Ile483=
XM_006712882.2:c.1449T=	XP_006712945.1:p.Ile483=
XM_011512231.1:c.1440T=	XP_011510533.1:p.Ile480=
XM_011512232.1:c.1428T=	XP_011510534.1:p.Ile476=
NM_014795.4:c.1449T= MANE Select	NP_055610.1:p.Ile483=
NM_001171653.2:c.1377T=	NP_001165124.1:p.Ile459=