Canonical Allele Identifier: CA1294885365

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399660C= , CM000664.2:g.144399660C=	GRCh38
NC_000002.11:g.145157227C= , CM000664.1:g.145157227C=	GRCh37
NC_000002.10:g.144873697C=	NCBI36
NG_016431.1:g.125732G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1376G=	ENSP00000508434.1:n.*1376G=
ENST00000440875.6:c.750G=	ENSP00000475553.3:p.Pro250=
ENST00000627532.3:c.1527G= MANE Select	ENSP00000487174.1:p.Pro509=
ENST00000636026.2:c.1527G=	ENSP00000490776.1:p.Pro509=
ENST00000636179.1:n.1496G=
ENST00000636413.1:c.1191G=	ENSP00000490508.1:p.Pro397=
ENST00000636471.1:c.1602G=	ENSP00000490317.1:p.Pro534=
ENST00000636732.2:c.*1244G=	ENSP00000490175.1:n.*1244G=
ENST00000636820.1:n.1627G=
ENST00000637045.1:c.1191G=	ENSP00000490141.1:p.Pro397=
ENST00000637267.2:c.1527G=	ENSP00000490293.2:p.Pro509=
ENST00000637304.1:c.1191G=	ENSP00000490872.1:p.Pro397=
ENST00000638007.1:c.1191G=	ENSP00000490723.1:p.Pro397=
ENST00000638087.1:c.1191G=	ENSP00000490673.1:p.Pro397=
ENST00000638128.1:c.750G=	ENSP00000490934.1:p.Pro250=
ENST00000675069.1:c.-133-810G=	ENSP00000502467.1:n.-133-810G=
ENST00000675145.1:n.2075G=
ENST00000303660.8:c.1524G=	ENSP00000302501.4:p.Pro508=
ENST00000409487.7:c.1527G=	ENSP00000386854.2:p.Pro509=
ENST00000419938.5:c.655+1539G=	ENSP00000394777.2:n.655+1539G=
ENST00000427902.5:c.1614G=	ENSP00000395496.2:p.Pro538=
ENST00000440875.5:c.1154-110G=	ENSP00000475553.2:n.1154-110G=
ENST00000539609.7:c.1455G=	ENSP00000443792.2:p.Pro485=
ENST00000558170.6:c.1527G=	ENSP00000454157.1:p.Pro509=
ENST00000627532.2:c.1527G=	ENSP00000487174.1:p.Pro509=
NM_001171653.1:c.1455G=	NP_001165124.1:p.Pro485=
NM_014795.3:c.1527G=	NP_055610.1:p.Pro509=
XM_006712881.2:c.1527G=	XP_006712944.1:p.Pro509=
XM_006712882.2:c.1527G=	XP_006712945.1:p.Pro509=
XM_011512231.1:c.1518G=	XP_011510533.1:p.Pro506=
XM_011512232.1:c.1506G=	XP_011510534.1:p.Pro502=
NM_014795.4:c.1527G= MANE Select	NP_055610.1:p.Pro509=
NM_001171653.2:c.1455G=	NP_001165124.1:p.Pro485=