Canonical Allele Identifier: CA1294880961

Gene: ZEB2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144388869A= , CM000664.2:g.144388869A=	GRCh38
NC_000002.11:g.145146436A= , CM000664.1:g.145146436A=	GRCh37
NC_000002.10:g.144862906A=	NCBI36
NG_016431.1:g.136523T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440875.6:c.*582T=	ENSP00000475553.3:n.*582T=
ENST00000627532.3:c.*582T= MANE Select	ENSP00000487174.1:n.*582T=
ENST00000636026.2:c.*506T=	ENSP00000490776.1:n.*506T=
ENST00000636179.1:n.4196T=
ENST00000636413.1:c.*582T=	ENSP00000490508.1:n.*582T=
ENST00000636471.1:c.*582T=	ENSP00000490317.1:n.*582T=
ENST00000636732.2:c.*3944T=	ENSP00000490175.1:n.*3944T=
ENST00000636820.1:n.4327T=
ENST00000637045.1:c.*582T=	ENSP00000490141.1:n.*582T=
ENST00000637304.1:c.*582T=	ENSP00000490872.1:n.*582T=
ENST00000638007.1:c.*582T=	ENSP00000490723.1:n.*582T=
ENST00000638087.1:c.*582T=	ENSP00000490673.1:n.*582T=
ENST00000638128.1:c.*582T=	ENSP00000490934.1:n.*582T=
ENST00000639389.1:c.151+7543T=	ENSP00000492572.1:n.151+7543T=
ENST00000647488.1:c.1447T=	ENSP00000494820.1:n.1447T=
ENST00000675069.1:c.*582T=	ENSP00000502467.1:n.*582T=
ENST00000409487.7:c.*582T=	ENSP00000386854.2:n.*582T=
ENST00000419938.5:c.*6T=	ENSP00000394777.2:n.*6T=
ENST00000627532.2:c.*582T=	ENSP00000487174.1:n.*582T=
NM_001171653.1:c.*582T=	NP_001165124.1:n.*582T=
NM_014795.3:c.*582T=	NP_055610.1:n.*582T=
XM_006712881.2:c.*582T=	XP_006712944.1:n.*582T=
XM_006712882.2:c.*582T=	XP_006712945.1:n.*582T=
XM_011512231.1:c.*582T=	XP_011510533.1:n.*582T=
XM_011512232.1:c.*582T=	XP_011510534.1:n.*582T=
NM_014795.4:c.*582T= MANE Select	NP_055610.1:n.*582T=
NM_001171653.2:c.*582T=	NP_001165124.1:n.*582T=