Canonical Allele Identifier: CA2586970133

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399901_144399907delinsCTCAGT , CM000664.2:g.144399901_144399907delinsCTCAGT	GRCh38
NC_000002.11:g.145157468_145157474delinsCTCAGT , CM000664.1:g.145157468_145157474delinsCTCAGT	GRCh37
NC_000002.10:g.144873938_144873944delinsCTCAGT	NCBI36
NG_016431.1:g.125485_125491delinsACTGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1129_*1135delinsACTGAG	ENSP00000508434.1:n.*1129_*1135delinsACTGAG
ENST00000440875.6:c.503_509delinsACTGAG	ENSP00000475553.3:p.Gly168AspfsTer2
ENST00000627532.3:c.1280_1286delinsACTGAG MANE Select	ENSP00000487174.1:p.Gly427AspfsTer2
ENST00000636026.2:c.1280_1286delinsACTGAG	ENSP00000490776.1:p.Gly427AspfsTer2
ENST00000636179.1:n.1249_1255delinsACTGAG
ENST00000636413.1:c.944_950delinsACTGAG	ENSP00000490508.1:p.Gly315AspfsTer2
ENST00000636471.1:c.1355_1361delinsACTGAG	ENSP00000490317.1:p.Gly452AspfsTer2
ENST00000636732.2:c.*997_*1003delinsACTGAG	ENSP00000490175.1:n.*997_*1003delinsACTGAG
ENST00000636820.1:n.1380_1386delinsACTGAG
ENST00000637045.1:c.944_950delinsACTGAG	ENSP00000490141.1:p.Gly315AspfsTer2
ENST00000637267.2:c.1280_1286delinsACTGAG	ENSP00000490293.2:p.Gly427AspfsTer2
ENST00000637304.1:c.944_950delinsACTGAG	ENSP00000490872.1:p.Gly315AspfsTer2
ENST00000638007.1:c.944_950delinsACTGAG	ENSP00000490723.1:p.Gly315AspfsTer2
ENST00000638087.1:c.944_950delinsACTGAG	ENSP00000490673.1:p.Gly315AspfsTer2
ENST00000638128.1:c.503_509delinsACTGAG	ENSP00000490934.1:p.Gly168AspfsTer2
ENST00000675069.1:c.-133-1057_-133-1051delinsACTGAG	ENSP00000502467.1:n.-133-1057_-133-1051delinsACTGAG
ENST00000675145.1:n.1828_1834delinsACTGAG
ENST00000303660.8:c.1277_1283delinsACTGAG	ENSP00000302501.4:p.Gly426AspfsTer2
ENST00000392861.6:c.1364_1370delinsACTGAG	ENSP00000376601.3:p.Gly455AspfsTer2
ENST00000409487.7:c.1280_1286delinsACTGAG	ENSP00000386854.2:p.Gly427AspfsTer2
ENST00000419938.5:c.655+1292_655+1298delinsACTGAG	ENSP00000394777.2:n.655+1292_655+1298delinsACTGAG
ENST00000427902.5:c.1367_1373delinsACTGAG	ENSP00000395496.2:p.Gly456AspfsTer2
ENST00000440875.5:c.1153+112_1153+118delinsACTGAG	ENSP00000475553.2:n.1153+112_1153+118delinsACTGAG
ENST00000539609.7:c.1208_1214delinsACTGAG	ENSP00000443792.2:p.Gly403AspfsTer2
ENST00000558170.6:c.1280_1286delinsACTGAG	ENSP00000454157.1:p.Gly427AspfsTer2
ENST00000627532.2:c.1280_1286delinsACTGAG	ENSP00000487174.1:p.Gly427AspfsTer2
NM_001171653.1:c.1208_1214delinsACTGAG	NP_001165124.1:p.Gly403AspfsTer2
NM_014795.3:c.1280_1286delinsACTGAG	NP_055610.1:p.Gly427AspfsTer2
XM_006712881.2:c.1280_1286delinsACTGAG	XP_006712944.1:p.Gly427AspfsTer2
XM_006712882.2:c.1280_1286delinsACTGAG	XP_006712945.1:p.Gly427AspfsTer2
XM_011512231.1:c.1271_1277delinsACTGAG	XP_011510533.1:p.Gly424AspfsTer2
XM_011512232.1:c.1259_1265delinsACTGAG	XP_011510534.1:p.Gly420AspfsTer2
NM_014795.4:c.1280_1286delinsACTGAG MANE Select	NP_055610.1:p.Gly427AspfsTer2
NM_001171653.2:c.1208_1214delinsACTGAG	NP_001165124.1:p.Gly403AspfsTer2