Canonical Allele Identifier: CA2538716308

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399824_144399825insGCCT , CM000664.2:g.144399824_144399825insGCCT	GRCh38
NC_000002.11:g.145157391_145157392insGCCT , CM000664.1:g.145157391_145157392insGCCT	GRCh37
NC_000002.10:g.144873861_144873862insGCCT	NCBI36
NG_016431.1:g.125569_125570insGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1213_*1214insGCAG	ENSP00000508434.1:n.*1213_*1214insGCAG
ENST00000440875.6:c.587_588insGCAG	ENSP00000475553.3:p.Ser196ArgfsTer3
ENST00000627532.3:c.1364_1365insGCAG MANE Select	ENSP00000487174.1:p.Ser455ArgfsTer3
ENST00000636026.2:c.1364_1365insGCAG	ENSP00000490776.1:p.Ser455ArgfsTer3
ENST00000636179.1:n.1333_1334insGCAG
ENST00000636413.1:c.1028_1029insGCAG	ENSP00000490508.1:p.Ser343ArgfsTer3
ENST00000636471.1:c.1439_1440insGCAG	ENSP00000490317.1:p.Ser480ArgfsTer3
ENST00000636732.2:c.*1081_*1082insGCAG	ENSP00000490175.1:n.*1081_*1082insGCAG
ENST00000636820.1:n.1464_1465insGCAG
ENST00000637045.1:c.1028_1029insGCAG	ENSP00000490141.1:p.Ser343ArgfsTer3
ENST00000637267.2:c.1364_1365insGCAG	ENSP00000490293.2:p.Ser455ArgfsTer3
ENST00000637304.1:c.1028_1029insGCAG	ENSP00000490872.1:p.Ser343ArgfsTer3
ENST00000638007.1:c.1028_1029insGCAG	ENSP00000490723.1:p.Ser343ArgfsTer3
ENST00000638087.1:c.1028_1029insGCAG	ENSP00000490673.1:p.Ser343ArgfsTer3
ENST00000638128.1:c.587_588insGCAG	ENSP00000490934.1:p.Ser196ArgfsTer3
ENST00000675069.1:c.-133-973_-133-972insGCAG	ENSP00000502467.1:n.-133-973_-133-972insGCAG
ENST00000675145.1:n.1912_1913insGCAG
ENST00000303660.8:c.1361_1362insGCAG	ENSP00000302501.4:p.Ser454ArgfsTer3
ENST00000409487.7:c.1364_1365insGCAG	ENSP00000386854.2:p.Ser455ArgfsTer3
ENST00000419938.5:c.655+1376_655+1377insGCAG	ENSP00000394777.2:n.655+1376_655+1377insGCAG
ENST00000427902.5:c.1451_1452insGCAG	ENSP00000395496.2:p.Ser484ArgfsTer3
ENST00000440875.5:c.1153+196_1153+197insGCAG	ENSP00000475553.2:n.1153+196_1153+197insGCAG
ENST00000539609.7:c.1292_1293insGCAG	ENSP00000443792.2:p.Ser431ArgfsTer3
ENST00000558170.6:c.1364_1365insGCAG	ENSP00000454157.1:p.Ser455ArgfsTer3
ENST00000627532.2:c.1364_1365insGCAG	ENSP00000487174.1:p.Ser455ArgfsTer3
NM_001171653.1:c.1292_1293insGCAG	NP_001165124.1:p.Ser431ArgfsTer3
NM_014795.3:c.1364_1365insGCAG	NP_055610.1:p.Ser455ArgfsTer3
XM_006712881.2:c.1364_1365insGCAG	XP_006712944.1:p.Ser455ArgfsTer3
XM_006712882.2:c.1364_1365insGCAG	XP_006712945.1:p.Ser455ArgfsTer3
XM_011512231.1:c.1355_1356insGCAG	XP_011510533.1:p.Ser452ArgfsTer3
XM_011512232.1:c.1343_1344insGCAG	XP_011510534.1:p.Ser448ArgfsTer3
NM_014795.4:c.1364_1365insGCAG MANE Select	NP_055610.1:p.Ser455ArgfsTer3
NM_001171653.2:c.1292_1293insGCAG	NP_001165124.1:p.Ser431ArgfsTer3