Canonical Allele Identifier: CA1294885256

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399324_144399325delinsGA , CM000664.2:g.144399324_144399325delinsGA	GRCh38
NC_000002.11:g.145156891_145156892delinsGA , CM000664.1:g.145156891_145156892delinsGA	GRCh37
NC_000002.10:g.144873361_144873362delinsGA	NCBI36
NG_016431.1:g.126067_126068delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1711_*1712delinsTC	ENSP00000508434.1:n.*1711_*1712delinsTC
ENST00000440875.6:c.1085_1086delinsTC	ENSP00000475553.3:p.Val362=
ENST00000627532.3:c.1862_1863delinsTC MANE Select	ENSP00000487174.1:p.Val621=
ENST00000636026.2:c.1862_1863delinsTC	ENSP00000490776.1:p.Val621=
ENST00000636179.1:n.1831_1832delinsTC
ENST00000636413.1:c.1526_1527delinsTC	ENSP00000490508.1:p.Val509=
ENST00000636471.1:c.1937_1938delinsTC	ENSP00000490317.1:p.Val646=
ENST00000636732.2:c.*1579_*1580delinsTC	ENSP00000490175.1:n.*1579_*1580delinsTC
ENST00000636820.1:n.1962_1963delinsTC
ENST00000637045.1:c.1526_1527delinsTC	ENSP00000490141.1:p.Val509=
ENST00000637304.1:c.1526_1527delinsTC	ENSP00000490872.1:p.Val509=
ENST00000638007.1:c.1526_1527delinsTC	ENSP00000490723.1:p.Val509=
ENST00000638087.1:c.1526_1527delinsTC	ENSP00000490673.1:p.Val509=
ENST00000638128.1:c.1085_1086delinsTC	ENSP00000490934.1:p.Val362=
ENST00000675069.1:c.-133-475_-133-474delinsTC	ENSP00000502467.1:n.-133-475_-133-474delinsTC
ENST00000675145.1:n.2410_2411delinsTC
ENST00000303660.8:c.1859_1860delinsTC	ENSP00000302501.4:p.Val620=
ENST00000409487.7:c.1862_1863delinsTC	ENSP00000386854.2:p.Val621=
ENST00000419938.5:c.655+1874_655+1875delinsTC	ENSP00000394777.2:n.655+1874_655+1875delinsTC
ENST00000427902.5:c.1949_1950delinsTC	ENSP00000395496.2:p.Val650=
ENST00000440875.5:c.1167+212_1167+213delinsTC	ENSP00000475553.2:n.1167+212_1167+213delinsTC
ENST00000539609.7:c.1790_1791delinsTC	ENSP00000443792.2:p.Val597=
ENST00000558170.6:c.1862_1863delinsTC	ENSP00000454157.1:p.Val621=
ENST00000627532.2:c.1862_1863delinsTC	ENSP00000487174.1:p.Val621=
NM_001171653.1:c.1790_1791delinsTC	NP_001165124.1:p.Val597=
NM_014795.3:c.1862_1863delinsTC	NP_055610.1:p.Val621=
XM_006712881.2:c.1862_1863delinsTC	XP_006712944.1:p.Val621=
XM_006712882.2:c.1862_1863delinsTC	XP_006712945.1:p.Val621=
XM_011512231.1:c.1853_1854delinsTC	XP_011510533.1:p.Val618=
XM_011512232.1:c.1841_1842delinsTC	XP_011510534.1:p.Val614=
NM_014795.4:c.1862_1863delinsTC MANE Select	NP_055610.1:p.Val621=
NM_001171653.2:c.1790_1791delinsTC	NP_001165124.1:p.Val597=