Canonical Allele Identifier: CA1294885344

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399600_144399601delinsCG , CM000664.2:g.144399600_144399601delinsCG	GRCh38
NC_000002.11:g.145157167_145157168delinsCG , CM000664.1:g.145157167_145157168delinsCG	GRCh37
NC_000002.10:g.144873637_144873638delinsCG	NCBI36
NG_016431.1:g.125791_125792delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1435_*1436delinsCG	ENSP00000508434.1:n.*1435_*1436delinsCG
ENST00000440875.6:c.809_810delinsCG	ENSP00000475553.3:p.Thr270=
ENST00000627532.3:c.1586_1587delinsCG MANE Select	ENSP00000487174.1:p.Thr529=
ENST00000636026.2:c.1586_1587delinsCG	ENSP00000490776.1:p.Thr529=
ENST00000636179.1:n.1555_1556delinsCG
ENST00000636413.1:c.1250_1251delinsCG	ENSP00000490508.1:p.Thr417=
ENST00000636471.1:c.1661_1662delinsCG	ENSP00000490317.1:p.Thr554=
ENST00000636732.2:c.*1303_*1304delinsCG	ENSP00000490175.1:n.*1303_*1304delinsCG
ENST00000636820.1:n.1686_1687delinsCG
ENST00000637045.1:c.1250_1251delinsCG	ENSP00000490141.1:p.Thr417=
ENST00000637267.2:c.1586_1587delinsCG	ENSP00000490293.2:p.Thr529=
ENST00000637304.1:c.1250_1251delinsCG	ENSP00000490872.1:p.Thr417=
ENST00000638007.1:c.1250_1251delinsCG	ENSP00000490723.1:p.Thr417=
ENST00000638087.1:c.1250_1251delinsCG	ENSP00000490673.1:p.Thr417=
ENST00000638128.1:c.809_810delinsCG	ENSP00000490934.1:p.Thr270=
ENST00000675069.1:c.-133-751_-133-750delinsCG	ENSP00000502467.1:n.-133-751_-133-750delinsCG
ENST00000675145.1:n.2134_2135delinsCG
ENST00000303660.8:c.1583_1584delinsCG	ENSP00000302501.4:p.Thr528=
ENST00000409487.7:c.1586_1587delinsCG	ENSP00000386854.2:p.Thr529=
ENST00000419938.5:c.655+1598_655+1599delinsCG	ENSP00000394777.2:n.655+1598_655+1599delinsCG
ENST00000427902.5:c.1673_1674delinsCG	ENSP00000395496.2:p.Thr558=
ENST00000440875.5:c.1154-51_1154-50delinsCG	ENSP00000475553.2:n.1154-51_1154-50delinsCG
ENST00000539609.7:c.1514_1515delinsCG	ENSP00000443792.2:p.Thr505=
ENST00000558170.6:c.1586_1587delinsCG	ENSP00000454157.1:p.Thr529=
ENST00000627532.2:c.1586_1587delinsCG	ENSP00000487174.1:p.Thr529=
NM_001171653.1:c.1514_1515delinsCG	NP_001165124.1:p.Thr505=
NM_014795.3:c.1586_1587delinsCG	NP_055610.1:p.Thr529=
XM_006712881.2:c.1586_1587delinsCG	XP_006712944.1:p.Thr529=
XM_006712882.2:c.1586_1587delinsCG	XP_006712945.1:p.Thr529=
XM_011512231.1:c.1577_1578delinsCG	XP_011510533.1:p.Thr526=
XM_011512232.1:c.1565_1566delinsCG	XP_011510534.1:p.Thr522=
NM_014795.4:c.1586_1587delinsCG MANE Select	NP_055610.1:p.Thr529=
NM_001171653.2:c.1514_1515delinsCG	NP_001165124.1:p.Thr505=