Canonical Allele Identifier: CA429218654

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161681A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404114A>T , CM000664.2:g.144404114A>T	GRCh38
NC_000002.11:g.145161681A>T , CM000664.1:g.145161681A>T	GRCh37
NC_000002.10:g.144878151A>T	NCBI36
NG_016431.1:g.121278T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*458T>A	ENSP00000508434.1:n.*458T>A
ENST00000440875.6:c.-169T>A	ENSP00000475553.3:n.-169T>A
ENST00000627532.3:c.609T>A MANE Select	ENSP00000487174.1:p.Thr203=
ENST00000636026.2:c.609T>A	ENSP00000490776.1:p.Thr203=
ENST00000636179.1:n.578T>A
ENST00000636413.1:c.273T>A	ENSP00000490508.1:p.Thr91=
ENST00000636471.1:c.609T>A	ENSP00000490317.1:p.Thr203=
ENST00000636732.2:c.*326T>A	ENSP00000490175.1:n.*326T>A
ENST00000636820.1:n.709T>A
ENST00000637045.1:c.273T>A	ENSP00000490141.1:p.Thr91=
ENST00000637267.2:c.609T>A	ENSP00000490293.2:p.Thr203=
ENST00000637304.1:c.273T>A	ENSP00000490872.1:p.Thr91=
ENST00000638007.1:c.273T>A	ENSP00000490723.1:p.Thr91=
ENST00000638087.1:c.273T>A	ENSP00000490673.1:p.Thr91=
ENST00000638128.1:c.-169T>A	ENSP00000490934.1:n.-169T>A
ENST00000675069.1:c.-133-5264T>A	ENSP00000502467.1:n.-133-5264T>A
ENST00000303660.8:c.606T>A	ENSP00000302501.4:p.Thr202=
ENST00000392861.6:c.693T>A	ENSP00000376601.3:p.Thr231=
ENST00000409487.7:c.609T>A	ENSP00000386854.2:p.Thr203=
ENST00000419938.5:c.348T>A	ENSP00000394777.2:p.Thr116=
ENST00000427902.5:c.696T>A	ENSP00000395496.2:p.Thr232=
ENST00000431672.4:c.537T>A	ENSP00000475267.2:p.Thr179=
ENST00000440875.5:c.594T>A	ENSP00000475553.2:p.Thr198=
ENST00000497268.1:n.555T>A
ENST00000539609.7:c.537T>A	ENSP00000443792.2:p.Thr179=
ENST00000558170.6:c.609T>A	ENSP00000454157.1:p.Thr203=
ENST00000627532.2:c.609T>A	ENSP00000487174.1:p.Thr203=
ENST00000627856.2:n.569T>A
NM_001171653.1:c.537T>A	NP_001165124.1:p.Thr179=
NM_014795.3:c.609T>A	NP_055610.1:p.Thr203=
XM_006712881.2:c.609T>A	XP_006712944.1:p.Thr203=
XM_006712882.2:c.609T>A	XP_006712945.1:p.Thr203=
XM_011512231.1:c.600T>A	XP_011510533.1:p.Thr200=
XM_011512232.1:c.588T>A	XP_011510534.1:p.Thr196=
NM_014795.4:c.609T>A MANE Select	NP_055610.1:p.Thr203=
NM_001171653.2:c.537T>A	NP_001165124.1:p.Thr179=