Canonical Allele Identifier: CA1294881417

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144390022_144390023delinsCT , CM000664.2:g.144390022_144390023delinsCT	GRCh38
NC_000002.11:g.145147589_145147590delinsCT , CM000664.1:g.145147589_145147590delinsCT	GRCh37
NC_000002.10:g.144864059_144864060delinsCT	NCBI36
NG_016431.1:g.135369_135370delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2922_*2923delinsAG	ENSP00000508434.1:n.*2922_*2923delinsAG
ENST00000440875.6:c.2296_2297delinsAG	ENSP00000475553.3:p.Arg766=
ENST00000627532.3:c.3073_3074delinsAG MANE Select	ENSP00000487174.1:p.Arg1025=
ENST00000636026.2:c.3073_3074delinsAG	ENSP00000490776.1:p.Arg1025=
ENST00000636179.1:n.3042_3043delinsAG
ENST00000636413.1:c.2737_2738delinsAG	ENSP00000490508.1:p.Arg913=
ENST00000636471.1:c.3148_3149delinsAG	ENSP00000490317.1:p.Arg1050=
ENST00000636732.2:c.*2790_*2791delinsAG	ENSP00000490175.1:n.*2790_*2791delinsAG
ENST00000636820.1:n.3173_3174delinsAG
ENST00000637045.1:c.2737_2738delinsAG	ENSP00000490141.1:p.Arg913=
ENST00000637304.1:c.2737_2738delinsAG	ENSP00000490872.1:p.Arg913=
ENST00000638007.1:c.2737_2738delinsAG	ENSP00000490723.1:p.Arg913=
ENST00000638087.1:c.2737_2738delinsAG	ENSP00000490673.1:p.Arg913=
ENST00000638128.1:c.2296_2297delinsAG	ENSP00000490934.1:p.Arg766=
ENST00000639389.1:c.151+6389_151+6390delinsAG	ENSP00000492572.1:n.151+6389_151+6390delinsAG
ENST00000647488.1:c.293_294delinsAG	ENSP00000494820.1:n.293_294delinsAG
ENST00000675069.1:c.604_605delinsAG	ENSP00000502467.1:p.Arg202=
ENST00000303660.8:c.3070_3071delinsAG	ENSP00000302501.4:p.Arg1024=
ENST00000409487.7:c.3073_3074delinsAG	ENSP00000386854.2:p.Arg1025=
ENST00000419938.5:c.656-1141_656-1140delinsAG	ENSP00000394777.2:n.656-1141_656-1140delinsAG
ENST00000539609.7:c.3001_3002delinsAG	ENSP00000443792.2:p.Arg1001=
ENST00000558170.6:c.3073_3074delinsAG	ENSP00000454157.1:p.Arg1025=
ENST00000627532.2:c.3073_3074delinsAG	ENSP00000487174.1:p.Arg1025=
NM_001171653.1:c.3001_3002delinsAG	NP_001165124.1:p.Arg1001=
NM_014795.3:c.3073_3074delinsAG	NP_055610.1:p.Arg1025=
XM_006712881.2:c.3073_3074delinsAG	XP_006712944.1:p.Arg1025=
XM_006712882.2:c.3073_3074delinsAG	XP_006712945.1:p.Arg1025=
XM_011512231.1:c.3064_3065delinsAG	XP_011510533.1:p.Arg1022=
XM_011512232.1:c.3052_3053delinsAG	XP_011510534.1:p.Arg1018=
NM_014795.4:c.3073_3074delinsAG MANE Select	NP_055610.1:p.Arg1025=
NM_001171653.2:c.3001_3002delinsAG	NP_001165124.1:p.Arg1001=