Canonical Allele Identifier: CA429218614

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161638G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404071G>T , CM000664.2:g.144404071G>T	GRCh38
NC_000002.11:g.145161638G>T , CM000664.1:g.145161638G>T	GRCh37
NC_000002.10:g.144878108G>T	NCBI36
NG_016431.1:g.121321C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*501C>A	ENSP00000508434.1:n.*501C>A
ENST00000440875.6:c.-126C>A	ENSP00000475553.3:n.-126C>A
ENST00000627532.3:c.652C>A MANE Select	ENSP00000487174.1:p.Arg218=
ENST00000636026.2:c.652C>A	ENSP00000490776.1:p.Arg218=
ENST00000636179.1:n.621C>A
ENST00000636413.1:c.316C>A	ENSP00000490508.1:p.Arg106=
ENST00000636471.1:c.652C>A	ENSP00000490317.1:p.Arg218=
ENST00000636732.2:c.*369C>A	ENSP00000490175.1:n.*369C>A
ENST00000636820.1:n.752C>A
ENST00000637045.1:c.316C>A	ENSP00000490141.1:p.Arg106=
ENST00000637267.2:c.652C>A	ENSP00000490293.2:p.Arg218=
ENST00000637304.1:c.316C>A	ENSP00000490872.1:p.Arg106=
ENST00000638007.1:c.316C>A	ENSP00000490723.1:p.Arg106=
ENST00000638087.1:c.316C>A	ENSP00000490673.1:p.Arg106=
ENST00000638128.1:c.-126C>A	ENSP00000490934.1:n.-126C>A
ENST00000675069.1:c.-133-5221C>A	ENSP00000502467.1:n.-133-5221C>A
ENST00000303660.8:c.649C>A	ENSP00000302501.4:p.Arg217=
ENST00000392861.6:c.736C>A	ENSP00000376601.3:p.Arg246=
ENST00000409487.7:c.652C>A	ENSP00000386854.2:p.Arg218=
ENST00000419938.5:c.391C>A	ENSP00000394777.2:p.Arg131=
ENST00000427902.5:c.739C>A	ENSP00000395496.2:p.Arg247=
ENST00000440875.5:c.637C>A	ENSP00000475553.2:p.Arg213=
ENST00000497268.1:n.598C>A
ENST00000539609.7:c.580C>A	ENSP00000443792.2:p.Arg194=
ENST00000558170.6:c.652C>A	ENSP00000454157.1:p.Arg218=
ENST00000627532.2:c.652C>A	ENSP00000487174.1:p.Arg218=
NM_001171653.1:c.580C>A	NP_001165124.1:p.Arg194=
NM_014795.3:c.652C>A	NP_055610.1:p.Arg218=
XM_006712881.2:c.652C>A	XP_006712944.1:p.Arg218=
XM_006712882.2:c.652C>A	XP_006712945.1:p.Arg218=
XM_011512231.1:c.643C>A	XP_011510533.1:p.Arg215=
XM_011512232.1:c.631C>A	XP_011510534.1:p.Arg211=
NM_014795.4:c.652C>A MANE Select	NP_055610.1:p.Arg218=
NM_001171653.2:c.580C>A	NP_001165124.1:p.Arg194=