Canonical Allele Identifier: CA2558241371

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399825_144399826insC , CM000664.2:g.144399825_144399826insC	GRCh38
NC_000002.11:g.145157392_145157393insC , CM000664.1:g.145157392_145157393insC	GRCh37
NC_000002.10:g.144873862_144873863insC	NCBI36
NG_016431.1:g.125566_125567insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1210_*1211insG	ENSP00000508434.1:n.*1210_*1211insG
ENST00000440875.6:c.584_585insG	ENSP00000475553.3:p.Asn195LysfsTer2
ENST00000627532.3:c.1361_1362insG MANE Select	ENSP00000487174.1:p.Asn454LysfsTer2
ENST00000636026.2:c.1361_1362insG	ENSP00000490776.1:p.Asn454LysfsTer2
ENST00000636179.1:n.1330_1331insG
ENST00000636413.1:c.1025_1026insG	ENSP00000490508.1:p.Asn342LysfsTer2
ENST00000636471.1:c.1436_1437insG	ENSP00000490317.1:p.Asn479LysfsTer2
ENST00000636732.2:c.*1078_*1079insG	ENSP00000490175.1:n.*1078_*1079insG
ENST00000636820.1:n.1461_1462insG
ENST00000637045.1:c.1025_1026insG	ENSP00000490141.1:p.Asn342LysfsTer2
ENST00000637267.2:c.1361_1362insG	ENSP00000490293.2:p.Asn454LysfsTer2
ENST00000637304.1:c.1025_1026insG	ENSP00000490872.1:p.Asn342LysfsTer2
ENST00000638007.1:c.1025_1026insG	ENSP00000490723.1:p.Asn342LysfsTer2
ENST00000638087.1:c.1025_1026insG	ENSP00000490673.1:p.Asn342LysfsTer2
ENST00000638128.1:c.584_585insG	ENSP00000490934.1:p.Asn195LysfsTer2
ENST00000675069.1:c.-133-976_-133-975insG	ENSP00000502467.1:n.-133-976_-133-975insG
ENST00000675145.1:n.1909_1910insG
ENST00000303660.8:c.1358_1359insG	ENSP00000302501.4:p.Asn453LysfsTer2
ENST00000409487.7:c.1361_1362insG	ENSP00000386854.2:p.Asn454LysfsTer2
ENST00000419938.5:c.655+1373_655+1374insG	ENSP00000394777.2:n.655+1373_655+1374insG
ENST00000427902.5:c.1448_1449insG	ENSP00000395496.2:p.Asn483LysfsTer2
ENST00000440875.5:c.1153+193_1153+194insG	ENSP00000475553.2:n.1153+193_1153+194insG
ENST00000539609.7:c.1289_1290insG	ENSP00000443792.2:p.Asn430LysfsTer2
ENST00000558170.6:c.1361_1362insG	ENSP00000454157.1:p.Asn454LysfsTer2
ENST00000627532.2:c.1361_1362insG	ENSP00000487174.1:p.Asn454LysfsTer2
NM_001171653.1:c.1289_1290insG	NP_001165124.1:p.Asn430LysfsTer2
NM_014795.3:c.1361_1362insG	NP_055610.1:p.Asn454LysfsTer2
XM_006712881.2:c.1361_1362insG	XP_006712944.1:p.Asn454LysfsTer2
XM_006712882.2:c.1361_1362insG	XP_006712945.1:p.Asn454LysfsTer2
XM_011512231.1:c.1352_1353insG	XP_011510533.1:p.Asn451LysfsTer2
XM_011512232.1:c.1340_1341insG	XP_011510534.1:p.Asn447LysfsTer2
NM_014795.4:c.1361_1362insG MANE Select	NP_055610.1:p.Asn454LysfsTer2
NM_001171653.2:c.1289_1290insG	NP_001165124.1:p.Asn430LysfsTer2