Canonical Allele Identifier: CA1294885064

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398883_144398884delinsAT , CM000664.2:g.144398883_144398884delinsAT	GRCh38
NC_000002.11:g.145156450_145156451delinsAT , CM000664.1:g.145156450_145156451delinsAT	GRCh37
NC_000002.10:g.144872920_144872921delinsAT	NCBI36
NG_016431.1:g.126508_126509delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2152_*2153delinsAT	ENSP00000508434.1:n.*2152_*2153delinsAT
ENST00000440875.6:c.1526_1527delinsAT	ENSP00000475553.3:p.Asn509=
ENST00000627532.3:c.2303_2304delinsAT MANE Select	ENSP00000487174.1:p.Asn768=
ENST00000636026.2:c.2303_2304delinsAT	ENSP00000490776.1:p.Asn768=
ENST00000636179.1:n.2272_2273delinsAT
ENST00000636413.1:c.1967_1968delinsAT	ENSP00000490508.1:p.Asn656=
ENST00000636471.1:c.2378_2379delinsAT	ENSP00000490317.1:p.Asn793=
ENST00000636732.2:c.*2020_*2021delinsAT	ENSP00000490175.1:n.*2020_*2021delinsAT
ENST00000636820.1:n.2403_2404delinsAT
ENST00000637045.1:c.1967_1968delinsAT	ENSP00000490141.1:p.Asn656=
ENST00000637304.1:c.1967_1968delinsAT	ENSP00000490872.1:p.Asn656=
ENST00000638007.1:c.1967_1968delinsAT	ENSP00000490723.1:p.Asn656=
ENST00000638087.1:c.1967_1968delinsAT	ENSP00000490673.1:p.Asn656=
ENST00000638128.1:c.1526_1527delinsAT	ENSP00000490934.1:p.Asn509=
ENST00000675069.1:c.-133-34_-133-33delinsAT	ENSP00000502467.1:n.-133-34_-133-33delinsAT
ENST00000675145.1:n.2851_2852delinsAT
ENST00000303660.8:c.2300_2301delinsAT	ENSP00000302501.4:p.Asn767=
ENST00000409487.7:c.2303_2304delinsAT	ENSP00000386854.2:p.Asn768=
ENST00000419938.5:c.655+2315_655+2316delinsAT	ENSP00000394777.2:n.655+2315_655+2316delinsAT
ENST00000440875.5:c.1167+653_1167+654delinsAT	ENSP00000475553.2:n.1167+653_1167+654delinsAT
ENST00000539609.7:c.2231_2232delinsAT	ENSP00000443792.2:p.Asn744=
ENST00000558170.6:c.2303_2304delinsAT	ENSP00000454157.1:p.Asn768=
ENST00000627532.2:c.2303_2304delinsAT	ENSP00000487174.1:p.Asn768=
NM_001171653.1:c.2231_2232delinsAT	NP_001165124.1:p.Asn744=
NM_014795.3:c.2303_2304delinsAT	NP_055610.1:p.Asn768=
XM_006712881.2:c.2303_2304delinsAT	XP_006712944.1:p.Asn768=
XM_006712882.2:c.2303_2304delinsAT	XP_006712945.1:p.Asn768=
XM_011512231.1:c.2294_2295delinsAT	XP_011510533.1:p.Asn765=
XM_011512232.1:c.2282_2283delinsAT	XP_011510534.1:p.Asn761=
NM_014795.4:c.2303_2304delinsAT MANE Select	NP_055610.1:p.Asn768=
NM_001171653.2:c.2231_2232delinsAT	NP_001165124.1:p.Asn744=