Canonical Allele Identifier: CA1294881326

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389767C= , CM000664.2:g.144389767C=	GRCh38
NC_000002.11:g.145147334C= , CM000664.1:g.145147334C=	GRCh37
NC_000002.10:g.144863804C=	NCBI36
NG_016431.1:g.135625G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3178G=	ENSP00000508434.1:n.*3178G=
ENST00000440875.6:c.2552G=	ENSP00000475553.3:p.Arg851=
ENST00000627532.3:c.3329G= MANE Select	ENSP00000487174.1:p.Arg1110=
ENST00000636026.2:c.3231-14G=	ENSP00000490776.1:n.3231-14G=
ENST00000636179.1:n.3298G=
ENST00000636413.1:c.2993G=	ENSP00000490508.1:p.Arg998=
ENST00000636471.1:c.3404G=	ENSP00000490317.1:p.Arg1135=
ENST00000636732.2:c.*3046G=	ENSP00000490175.1:n.*3046G=
ENST00000636820.1:n.3429G=
ENST00000637045.1:c.2993G=	ENSP00000490141.1:p.Arg998=
ENST00000637304.1:c.2993G=	ENSP00000490872.1:p.Arg998=
ENST00000638007.1:c.2993G=	ENSP00000490723.1:p.Arg998=
ENST00000638087.1:c.2993G=	ENSP00000490673.1:p.Arg998=
ENST00000638128.1:c.2552G=	ENSP00000490934.1:p.Arg851=
ENST00000639389.1:c.151+6645G=	ENSP00000492572.1:n.151+6645G=
ENST00000647488.1:c.549G=	ENSP00000494820.1:n.549G=
ENST00000675069.1:c.860G=	ENSP00000502467.1:p.Arg287=
ENST00000303660.8:c.3326G=	ENSP00000302501.4:p.Arg1109=
ENST00000409487.7:c.3329G=	ENSP00000386854.2:p.Arg1110=
ENST00000419938.5:c.656-885G=	ENSP00000394777.2:n.656-885G=
ENST00000539609.7:c.3257G=	ENSP00000443792.2:p.Arg1086=
ENST00000558170.6:c.3329G=	ENSP00000454157.1:p.Arg1110=
ENST00000627532.2:c.3329G=	ENSP00000487174.1:p.Arg1110=
NM_001171653.1:c.3257G=	NP_001165124.1:p.Arg1086=
NM_014795.3:c.3329G=	NP_055610.1:p.Arg1110=
XM_006712881.2:c.3329G=	XP_006712944.1:p.Arg1110=
XM_006712882.2:c.3329G=	XP_006712945.1:p.Arg1110=
XM_011512231.1:c.3320G=	XP_011510533.1:p.Arg1107=
XM_011512232.1:c.3308G=	XP_011510534.1:p.Arg1103=
NM_014795.4:c.3329G= MANE Select	NP_055610.1:p.Arg1110=
NM_001171653.2:c.3257G=	NP_001165124.1:p.Arg1086=