Canonical Allele Identifier: CA1294881288

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389660C= , CM000664.2:g.144389660C=	GRCh38
NC_000002.11:g.145147227C= , CM000664.1:g.145147227C=	GRCh37
NC_000002.10:g.144863697C=	NCBI36
NG_016431.1:g.135732G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3285G=	ENSP00000508434.1:n.*3285G=
ENST00000440875.6:c.2659G=	ENSP00000475553.3:p.Asp887=
ENST00000627532.3:c.3436G= MANE Select	ENSP00000487174.1:p.Asp1146=
ENST00000636026.2:c.3324G=	ENSP00000490776.1:p.Arg1108=
ENST00000636179.1:n.3405G=
ENST00000636413.1:c.3100G=	ENSP00000490508.1:p.Asp1034=
ENST00000636471.1:c.3511G=	ENSP00000490317.1:p.Asp1171=
ENST00000636732.2:c.*3153G=	ENSP00000490175.1:n.*3153G=
ENST00000636820.1:n.3536G=
ENST00000637045.1:c.3100G=	ENSP00000490141.1:p.Asp1034=
ENST00000637304.1:c.3100G=	ENSP00000490872.1:p.Asp1034=
ENST00000638007.1:c.3100G=	ENSP00000490723.1:p.Asp1034=
ENST00000638087.1:c.3100G=	ENSP00000490673.1:p.Asp1034=
ENST00000638128.1:c.2659G=	ENSP00000490934.1:p.Asp887=
ENST00000639389.1:c.151+6752G=	ENSP00000492572.1:n.151+6752G=
ENST00000647488.1:c.656G=	ENSP00000494820.1:n.656G=
ENST00000675069.1:c.967G=	ENSP00000502467.1:p.Asp323=
ENST00000303660.8:c.3433G=	ENSP00000302501.4:p.Asp1145=
ENST00000409487.7:c.3436G=	ENSP00000386854.2:p.Asp1146=
ENST00000419938.5:c.656-778G=	ENSP00000394777.2:n.656-778G=
ENST00000539609.7:c.3364G=	ENSP00000443792.2:p.Asp1122=
ENST00000558170.6:c.3436G=	ENSP00000454157.1:p.Asp1146=
ENST00000627532.2:c.3436G=	ENSP00000487174.1:p.Asp1146=
NM_001171653.1:c.3364G=	NP_001165124.1:p.Asp1122=
NM_014795.3:c.3436G=	NP_055610.1:p.Asp1146=
XM_006712881.2:c.3436G=	XP_006712944.1:p.Asp1146=
XM_006712882.2:c.3436G=	XP_006712945.1:p.Asp1146=
XM_011512231.1:c.3427G=	XP_011510533.1:p.Asp1143=
XM_011512232.1:c.3415G=	XP_011510534.1:p.Asp1139=
NM_014795.4:c.3436G= MANE Select	NP_055610.1:p.Asp1146=
NM_001171653.2:c.3364G=	NP_001165124.1:p.Asp1122=