Canonical Allele Identifier: CA1294885215

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399233A= , CM000664.2:g.144399233A=	GRCh38
NC_000002.11:g.145156800A= , CM000664.1:g.145156800A=	GRCh37
NC_000002.10:g.144873270A=	NCBI36
NG_016431.1:g.126159T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*1803T=	ENSP00000508434.1:n.*1803T=
ENST00000440875.6:c.1177T=	ENSP00000475553.3:p.Tyr393=
ENST00000627532.3:c.1954T= MANE Select	ENSP00000487174.1:p.Tyr652=
ENST00000636026.2:c.1954T=	ENSP00000490776.1:p.Tyr652=
ENST00000636179.1:n.1923T=
ENST00000636413.1:c.1618T=	ENSP00000490508.1:p.Tyr540=
ENST00000636471.1:c.2029T=	ENSP00000490317.1:p.Tyr677=
ENST00000636732.2:c.*1671T=	ENSP00000490175.1:n.*1671T=
ENST00000636820.1:n.2054T=
ENST00000637045.1:c.1618T=	ENSP00000490141.1:p.Tyr540=
ENST00000637304.1:c.1618T=	ENSP00000490872.1:p.Tyr540=
ENST00000638007.1:c.1618T=	ENSP00000490723.1:p.Tyr540=
ENST00000638087.1:c.1618T=	ENSP00000490673.1:p.Tyr540=
ENST00000638128.1:c.1177T=	ENSP00000490934.1:p.Tyr393=
ENST00000675069.1:c.-133-383T=	ENSP00000502467.1:n.-133-383T=
ENST00000675145.1:n.2502T=
ENST00000303660.8:c.1951T=	ENSP00000302501.4:p.Tyr651=
ENST00000409487.7:c.1954T=	ENSP00000386854.2:p.Tyr652=
ENST00000419938.5:c.655+1966T=	ENSP00000394777.2:n.655+1966T=
ENST00000427902.5:c.2041T=	ENSP00000395496.2:p.Tyr681=
ENST00000440875.5:c.1167+304T=	ENSP00000475553.2:n.1167+304T=
ENST00000539609.7:c.1882T=	ENSP00000443792.2:p.Tyr628=
ENST00000558170.6:c.1954T=	ENSP00000454157.1:p.Tyr652=
ENST00000627532.2:c.1954T=	ENSP00000487174.1:p.Tyr652=
NM_001171653.1:c.1882T=	NP_001165124.1:p.Tyr628=
NM_014795.3:c.1954T=	NP_055610.1:p.Tyr652=
XM_006712881.2:c.1954T=	XP_006712944.1:p.Tyr652=
XM_006712882.2:c.1954T=	XP_006712945.1:p.Tyr652=
XM_011512231.1:c.1945T=	XP_011510533.1:p.Tyr649=
XM_011512232.1:c.1933T=	XP_011510534.1:p.Tyr645=
NM_014795.4:c.1954T= MANE Select	NP_055610.1:p.Tyr652=
NM_001171653.2:c.1882T=	NP_001165124.1:p.Tyr628=