Canonical Allele Identifier: CA1294881376

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389888_144389894delinsACGAGCC , CM000664.2:g.144389888_144389894delinsACGAGCC	GRCh38
NC_000002.11:g.145147455_145147461delinsACGAGCC , CM000664.1:g.145147455_145147461delinsACGAGCC	GRCh37
NC_000002.10:g.144863925_144863931delinsACGAGCC	NCBI36
NG_016431.1:g.135498_135504delinsGGCTCGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3051_*3057delinsGGCTCGT	ENSP00000508434.1:n.*3051_*3057delinsGGCTCGT
ENST00000440875.6:c.2425_2431delinsGGCTCGT	ENSP00000475553.3:p.Gly809=
ENST00000627532.3:c.3202_3208delinsGGCTCGT MANE Select	ENSP00000487174.1:p.Gly1068=
ENST00000636026.2:c.3202_3208delinsGGCTCGT	ENSP00000490776.1:p.Gly1068=
ENST00000636179.1:n.3171_3177delinsGGCTCGT
ENST00000636413.1:c.2866_2872delinsGGCTCGT	ENSP00000490508.1:p.Gly956=
ENST00000636471.1:c.3277_3283delinsGGCTCGT	ENSP00000490317.1:p.Gly1093=
ENST00000636732.2:c.*2919_*2925delinsGGCTCGT	ENSP00000490175.1:n.*2919_*2925delinsGGCTCGT
ENST00000636820.1:n.3302_3308delinsGGCTCGT
ENST00000637045.1:c.2866_2872delinsGGCTCGT	ENSP00000490141.1:p.Gly956=
ENST00000637304.1:c.2866_2872delinsGGCTCGT	ENSP00000490872.1:p.Gly956=
ENST00000638007.1:c.2866_2872delinsGGCTCGT	ENSP00000490723.1:p.Gly956=
ENST00000638087.1:c.2866_2872delinsGGCTCGT	ENSP00000490673.1:p.Gly956=
ENST00000638128.1:c.2425_2431delinsGGCTCGT	ENSP00000490934.1:p.Gly809=
ENST00000639389.1:c.151+6518_151+6524delinsGGCTCGT	ENSP00000492572.1:n.151+6518_151+6524delinsGGCTCGT
ENST00000647488.1:c.422_428delinsGGCTCGT	ENSP00000494820.1:n.422_428delinsGGCTCGT
ENST00000675069.1:c.733_739delinsGGCTCGT	ENSP00000502467.1:p.Gly245=
ENST00000303660.8:c.3199_3205delinsGGCTCGT	ENSP00000302501.4:p.Gly1067=
ENST00000409487.7:c.3202_3208delinsGGCTCGT	ENSP00000386854.2:p.Gly1068=
ENST00000419938.5:c.656-1012_656-1006delinsGGCTCGT	ENSP00000394777.2:n.656-1012_656-1006delinsGGCTCGT
ENST00000539609.7:c.3130_3136delinsGGCTCGT	ENSP00000443792.2:p.Gly1044=
ENST00000558170.6:c.3202_3208delinsGGCTCGT	ENSP00000454157.1:p.Gly1068=
ENST00000627532.2:c.3202_3208delinsGGCTCGT	ENSP00000487174.1:p.Gly1068=
NM_001171653.1:c.3130_3136delinsGGCTCGT	NP_001165124.1:p.Gly1044=
NM_014795.3:c.3202_3208delinsGGCTCGT	NP_055610.1:p.Gly1068=
XM_006712881.2:c.3202_3208delinsGGCTCGT	XP_006712944.1:p.Gly1068=
XM_006712882.2:c.3202_3208delinsGGCTCGT	XP_006712945.1:p.Gly1068=
XM_011512231.1:c.3193_3199delinsGGCTCGT	XP_011510533.1:p.Gly1065=
XM_011512232.1:c.3181_3187delinsGGCTCGT	XP_011510534.1:p.Gly1061=
NM_014795.4:c.3202_3208delinsGGCTCGT MANE Select	NP_055610.1:p.Gly1068=
NM_001171653.2:c.3130_3136delinsGGCTCGT	NP_001165124.1:p.Gly1044=