Canonical Allele Identifier: CA1294881313

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389733G= , CM000664.2:g.144389733G=	GRCh38
NC_000002.11:g.145147300G= , CM000664.1:g.145147300G=	GRCh37
NC_000002.10:g.144863770G=	NCBI36
NG_016431.1:g.135659C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3212C=	ENSP00000508434.1:n.*3212C=
ENST00000440875.6:c.2586C=	ENSP00000475553.3:p.Tyr862=
ENST00000627532.3:c.3363C= MANE Select	ENSP00000487174.1:p.Tyr1121=
ENST00000636026.2:c.3251C=	ENSP00000490776.1:p.Thr1084=
ENST00000636179.1:n.3332C=
ENST00000636413.1:c.3027C=	ENSP00000490508.1:p.Tyr1009=
ENST00000636471.1:c.3438C=	ENSP00000490317.1:p.Tyr1146=
ENST00000636732.2:c.*3080C=	ENSP00000490175.1:n.*3080C=
ENST00000636820.1:n.3463C=
ENST00000637045.1:c.3027C=	ENSP00000490141.1:p.Tyr1009=
ENST00000637304.1:c.3027C=	ENSP00000490872.1:p.Tyr1009=
ENST00000638007.1:c.3027C=	ENSP00000490723.1:p.Tyr1009=
ENST00000638087.1:c.3027C=	ENSP00000490673.1:p.Tyr1009=
ENST00000638128.1:c.2586C=	ENSP00000490934.1:p.Tyr862=
ENST00000639389.1:c.151+6679C=	ENSP00000492572.1:n.151+6679C=
ENST00000647488.1:c.583C=	ENSP00000494820.1:n.583C=
ENST00000675069.1:c.894C=	ENSP00000502467.1:p.Tyr298=
ENST00000303660.8:c.3360C=	ENSP00000302501.4:p.Tyr1120=
ENST00000409487.7:c.3363C=	ENSP00000386854.2:p.Tyr1121=
ENST00000419938.5:c.656-851C=	ENSP00000394777.2:n.656-851C=
ENST00000539609.7:c.3291C=	ENSP00000443792.2:p.Tyr1097=
ENST00000558170.6:c.3363C=	ENSP00000454157.1:p.Tyr1121=
ENST00000627532.2:c.3363C=	ENSP00000487174.1:p.Tyr1121=
NM_001171653.1:c.3291C=	NP_001165124.1:p.Tyr1097=
NM_014795.3:c.3363C=	NP_055610.1:p.Tyr1121=
XM_006712881.2:c.3363C=	XP_006712944.1:p.Tyr1121=
XM_006712882.2:c.3363C=	XP_006712945.1:p.Tyr1121=
XM_011512231.1:c.3354C=	XP_011510533.1:p.Tyr1118=
XM_011512232.1:c.3342C=	XP_011510534.1:p.Tyr1114=
NM_014795.4:c.3363C= MANE Select	NP_055610.1:p.Tyr1121=
NM_001171653.2:c.3291C=	NP_001165124.1:p.Tyr1097=