Canonical Allele Identifier: CA2586969982

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144389968_144389971delinsC , CM000664.2:g.144389968_144389971delinsC	GRCh38
NC_000002.11:g.145147535_145147538delinsC , CM000664.1:g.145147535_145147538delinsC	GRCh37
NC_000002.10:g.144864005_144864008delinsC	NCBI36
NG_016431.1:g.135421_135424delinsG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2974_*2977delinsG	ENSP00000508434.1:n.*2974_*2977delinsG
ENST00000440875.6:c.2348_2351delinsG	ENSP00000475553.3:p.Leu783_Ile784delinsArg
ENST00000627532.3:c.3125_3128delinsG MANE Select	ENSP00000487174.1:p.Leu1042_Ile1043delinsArg
ENST00000636026.2:c.3125_3128delinsG	ENSP00000490776.1:p.Leu1042_Ile1043delinsArg
ENST00000636179.1:n.3094_3097delinsG
ENST00000636413.1:c.2789_2792delinsG	ENSP00000490508.1:p.Leu930_Ile931delinsArg
ENST00000636471.1:c.3200_3203delinsG	ENSP00000490317.1:p.Leu1067_Ile1068delinsArg
ENST00000636732.2:c.*2842_*2845delinsG	ENSP00000490175.1:n.*2842_*2845delinsG
ENST00000636820.1:n.3225_3228delinsG
ENST00000637045.1:c.2789_2792delinsG	ENSP00000490141.1:p.Leu930_Ile931delinsArg
ENST00000637304.1:c.2789_2792delinsG	ENSP00000490872.1:p.Leu930_Ile931delinsArg
ENST00000638007.1:c.2789_2792delinsG	ENSP00000490723.1:p.Leu930_Ile931delinsArg
ENST00000638087.1:c.2789_2792delinsG	ENSP00000490673.1:p.Leu930_Ile931delinsArg
ENST00000638128.1:c.2348_2351delinsG	ENSP00000490934.1:p.Leu783_Ile784delinsArg
ENST00000639389.1:c.151+6441_151+6444delinsG	ENSP00000492572.1:n.151+6441_151+6444delinsG
ENST00000647488.1:c.345_348delinsG	ENSP00000494820.1:n.345_348delinsG
ENST00000675069.1:c.656_659delinsG	ENSP00000502467.1:p.Leu219_Ile220delinsArg
ENST00000303660.8:c.3122_3125delinsG	ENSP00000302501.4:p.Leu1041_Ile1042delinsArg
ENST00000409487.7:c.3125_3128delinsG	ENSP00000386854.2:p.Leu1042_Ile1043delinsArg
ENST00000419938.5:c.656-1089_656-1086delinsG	ENSP00000394777.2:n.656-1089_656-1086delinsG
ENST00000539609.7:c.3053_3056delinsG	ENSP00000443792.2:p.Leu1018_Ile1019delinsArg
ENST00000558170.6:c.3125_3128delinsG	ENSP00000454157.1:p.Leu1042_Ile1043delinsArg
ENST00000627532.2:c.3125_3128delinsG	ENSP00000487174.1:p.Leu1042_Ile1043delinsArg
NM_001171653.1:c.3053_3056delinsG	NP_001165124.1:p.Leu1018_Ile1019delinsArg
NM_014795.3:c.3125_3128delinsG	NP_055610.1:p.Leu1042_Ile1043delinsArg
XM_006712881.2:c.3125_3128delinsG	XP_006712944.1:p.Leu1042_Ile1043delinsArg
XM_006712882.2:c.3125_3128delinsG	XP_006712945.1:p.Leu1042_Ile1043delinsArg
XM_011512231.1:c.3116_3119delinsG	XP_011510533.1:p.Leu1039_Ile1040delinsArg
XM_011512232.1:c.3104_3107delinsG	XP_011510534.1:p.Leu1035_Ile1036delinsArg
NM_014795.4:c.3125_3128delinsG MANE Select	NP_055610.1:p.Leu1042_Ile1043delinsArg
NM_001171653.2:c.3053_3056delinsG	NP_001165124.1:p.Leu1018_Ile1019delinsArg