Canonical Allele Identifier: CA1294885351

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399630_144399631delinsAT , CM000664.2:g.144399630_144399631delinsAT	GRCh38
NC_000002.11:g.145157197_145157198delinsAT , CM000664.1:g.145157197_145157198delinsAT	GRCh37
NC_000002.10:g.144873667_144873668delinsAT	NCBI36
NG_016431.1:g.125761_125762delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1405_*1406delinsAT	ENSP00000508434.1:n.*1405_*1406delinsAT
ENST00000440875.6:c.779_780delinsAT	ENSP00000475553.3:p.Asn260=
ENST00000627532.3:c.1556_1557delinsAT MANE Select	ENSP00000487174.1:p.Asn519=
ENST00000636026.2:c.1556_1557delinsAT	ENSP00000490776.1:p.Asn519=
ENST00000636179.1:n.1525_1526delinsAT
ENST00000636413.1:c.1220_1221delinsAT	ENSP00000490508.1:p.Asn407=
ENST00000636471.1:c.1631_1632delinsAT	ENSP00000490317.1:p.Asn544=
ENST00000636732.2:c.*1273_*1274delinsAT	ENSP00000490175.1:n.*1273_*1274delinsAT
ENST00000636820.1:n.1656_1657delinsAT
ENST00000637045.1:c.1220_1221delinsAT	ENSP00000490141.1:p.Asn407=
ENST00000637267.2:c.1556_1557delinsAT	ENSP00000490293.2:p.Asn519=
ENST00000637304.1:c.1220_1221delinsAT	ENSP00000490872.1:p.Asn407=
ENST00000638007.1:c.1220_1221delinsAT	ENSP00000490723.1:p.Asn407=
ENST00000638087.1:c.1220_1221delinsAT	ENSP00000490673.1:p.Asn407=
ENST00000638128.1:c.779_780delinsAT	ENSP00000490934.1:p.Asn260=
ENST00000675069.1:c.-133-781_-133-780delinsAT	ENSP00000502467.1:n.-133-781_-133-780delinsAT
ENST00000675145.1:n.2104_2105delinsAT
ENST00000303660.8:c.1553_1554delinsAT	ENSP00000302501.4:p.Asn518=
ENST00000409487.7:c.1556_1557delinsAT	ENSP00000386854.2:p.Asn519=
ENST00000419938.5:c.655+1568_655+1569delinsAT	ENSP00000394777.2:n.655+1568_655+1569delinsAT
ENST00000427902.5:c.1643_1644delinsAT	ENSP00000395496.2:p.Asn548=
ENST00000440875.5:c.1154-81_1154-80delinsAT	ENSP00000475553.2:n.1154-81_1154-80delinsAT
ENST00000539609.7:c.1484_1485delinsAT	ENSP00000443792.2:p.Asn495=
ENST00000558170.6:c.1556_1557delinsAT	ENSP00000454157.1:p.Asn519=
ENST00000627532.2:c.1556_1557delinsAT	ENSP00000487174.1:p.Asn519=
NM_001171653.1:c.1484_1485delinsAT	NP_001165124.1:p.Asn495=
NM_014795.3:c.1556_1557delinsAT	NP_055610.1:p.Asn519=
XM_006712881.2:c.1556_1557delinsAT	XP_006712944.1:p.Asn519=
XM_006712882.2:c.1556_1557delinsAT	XP_006712945.1:p.Asn519=
XM_011512231.1:c.1547_1548delinsAT	XP_011510533.1:p.Asn516=
XM_011512232.1:c.1535_1536delinsAT	XP_011510534.1:p.Asn512=
NM_014795.4:c.1556_1557delinsAT MANE Select	NP_055610.1:p.Asn519=
NM_001171653.2:c.1484_1485delinsAT	NP_001165124.1:p.Asn495=