Canonical Allele Identifier: CA2577152072

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389749_144389751del , CM000664.2:g.144389749_144389751del	GRCh38
NC_000002.11:g.145147316_145147318del , CM000664.1:g.145147316_145147318del	GRCh37
NC_000002.10:g.144863786_144863788del	NCBI36
NG_016431.1:g.135641_135643del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*3194_*3196del	ENSP00000508434.1:n.*3194_*3196del
ENST00000440875.6:c.2568_2570del	ENSP00000475553.3:p.Ile857del
ENST00000627532.3:c.3345_3347del MANE Select	ENSP00000487174.1:p.Ile1116del
ENST00000636026.2:c.3233_3235del	ENSP00000490776.1:p.Ala1078_Leu1079delinsVal
ENST00000636179.1:n.3314_3316del
ENST00000636413.1:c.3009_3011del	ENSP00000490508.1:p.Ile1004del
ENST00000636471.1:c.3420_3422del	ENSP00000490317.1:p.Ile1141del
ENST00000636732.2:c.*3062_*3064del	ENSP00000490175.1:n.*3062_*3064del
ENST00000636820.1:n.3445_3447del
ENST00000637045.1:c.3009_3011del	ENSP00000490141.1:p.Ile1004del
ENST00000637304.1:c.3009_3011del	ENSP00000490872.1:p.Ile1004del
ENST00000638007.1:c.3009_3011del	ENSP00000490723.1:p.Ile1004del
ENST00000638087.1:c.3009_3011del	ENSP00000490673.1:p.Ile1004del
ENST00000638128.1:c.2568_2570del	ENSP00000490934.1:p.Ile857del
ENST00000639389.1:c.151+6661_151+6663del	ENSP00000492572.1:n.151+6661_151+6663del
ENST00000647488.1:c.565_567del	ENSP00000494820.1:n.565_567del
ENST00000675069.1:c.876_878del	ENSP00000502467.1:p.Ile293del
ENST00000303660.8:c.3342_3344del	ENSP00000302501.4:p.Ile1115del
ENST00000409487.7:c.3345_3347del	ENSP00000386854.2:p.Ile1116del
ENST00000419938.5:c.656-869_656-867del	ENSP00000394777.2:n.656-869_656-867del
ENST00000539609.7:c.3273_3275del	ENSP00000443792.2:p.Ile1092del
ENST00000558170.6:c.3345_3347del	ENSP00000454157.1:p.Ile1116del
ENST00000627532.2:c.3345_3347del	ENSP00000487174.1:p.Ile1116del
NM_001171653.1:c.3273_3275del	NP_001165124.1:p.Ile1092del
NM_014795.3:c.3345_3347del	NP_055610.1:p.Ile1116del
XM_006712881.2:c.3345_3347del	XP_006712944.1:p.Ile1116del
XM_006712882.2:c.3345_3347del	XP_006712945.1:p.Ile1116del
XM_011512231.1:c.3336_3338del	XP_011510533.1:p.Ile1113del
XM_011512232.1:c.3324_3326del	XP_011510534.1:p.Ile1109del
NM_014795.4:c.3345_3347del MANE Select	NP_055610.1:p.Ile1116del
NM_001171653.2:c.3273_3275del	NP_001165124.1:p.Ile1092del