Canonical Allele Identifier: CA1294885226

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399265_144399266delinsGA , CM000664.2:g.144399265_144399266delinsGA	GRCh38
NC_000002.11:g.145156832_145156833delinsGA , CM000664.1:g.145156832_145156833delinsGA	GRCh37
NC_000002.10:g.144873302_144873303delinsGA	NCBI36
NG_016431.1:g.126126_126127delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1770_*1771delinsTC	ENSP00000508434.1:n.*1770_*1771delinsTC
ENST00000440875.6:c.1144_1145delinsTC	ENSP00000475553.3:p.Ser382=
ENST00000627532.3:c.1921_1922delinsTC MANE Select	ENSP00000487174.1:p.Ser641=
ENST00000636026.2:c.1921_1922delinsTC	ENSP00000490776.1:p.Ser641=
ENST00000636179.1:n.1890_1891delinsTC
ENST00000636413.1:c.1585_1586delinsTC	ENSP00000490508.1:p.Ser529=
ENST00000636471.1:c.1996_1997delinsTC	ENSP00000490317.1:p.Ser666=
ENST00000636732.2:c.*1638_*1639delinsTC	ENSP00000490175.1:n.*1638_*1639delinsTC
ENST00000636820.1:n.2021_2022delinsTC
ENST00000637045.1:c.1585_1586delinsTC	ENSP00000490141.1:p.Ser529=
ENST00000637304.1:c.1585_1586delinsTC	ENSP00000490872.1:p.Ser529=
ENST00000638007.1:c.1585_1586delinsTC	ENSP00000490723.1:p.Ser529=
ENST00000638087.1:c.1585_1586delinsTC	ENSP00000490673.1:p.Ser529=
ENST00000638128.1:c.1144_1145delinsTC	ENSP00000490934.1:p.Ser382=
ENST00000675069.1:c.-133-416_-133-415delinsTC	ENSP00000502467.1:n.-133-416_-133-415delinsTC
ENST00000675145.1:n.2469_2470delinsTC
ENST00000303660.8:c.1918_1919delinsTC	ENSP00000302501.4:p.Ser640=
ENST00000409487.7:c.1921_1922delinsTC	ENSP00000386854.2:p.Ser641=
ENST00000419938.5:c.655+1933_655+1934delinsTC	ENSP00000394777.2:n.655+1933_655+1934delinsTC
ENST00000427902.5:c.2008_2009delinsTC	ENSP00000395496.2:p.Ser670=
ENST00000440875.5:c.1167+271_1167+272delinsTC	ENSP00000475553.2:n.1167+271_1167+272delinsTC
ENST00000539609.7:c.1849_1850delinsTC	ENSP00000443792.2:p.Ser617=
ENST00000558170.6:c.1921_1922delinsTC	ENSP00000454157.1:p.Ser641=
ENST00000627532.2:c.1921_1922delinsTC	ENSP00000487174.1:p.Ser641=
NM_001171653.1:c.1849_1850delinsTC	NP_001165124.1:p.Ser617=
NM_014795.3:c.1921_1922delinsTC	NP_055610.1:p.Ser641=
XM_006712881.2:c.1921_1922delinsTC	XP_006712944.1:p.Ser641=
XM_006712882.2:c.1921_1922delinsTC	XP_006712945.1:p.Ser641=
XM_011512231.1:c.1912_1913delinsTC	XP_011510533.1:p.Ser638=
XM_011512232.1:c.1900_1901delinsTC	XP_011510534.1:p.Ser634=
NM_014795.4:c.1921_1922delinsTC MANE Select	NP_055610.1:p.Ser641=
NM_001171653.2:c.1849_1850delinsTC	NP_001165124.1:p.Ser617=