Canonical Allele Identifier: CA348714668

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161538G>A (hg19) ; chr2:g.144403971G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403971G>A , CM000664.2:g.144403971G>A	GRCh38
NC_000002.11:g.145161538G>A , CM000664.1:g.145161538G>A	GRCh37
NC_000002.10:g.144878008G>A	NCBI36
NG_016431.1:g.121421C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*601C>T	ENSP00000508434.1:n.*601C>T
ENST00000440875.6:c.-26C>T	ENSP00000475553.3:n.-26C>T
ENST00000627532.3:c.752C>T MANE Select	ENSP00000487174.1:p.Ala251Val
ENST00000636026.2:c.752C>T	ENSP00000490776.1:p.Ala251Val
ENST00000636179.1:n.721C>T
ENST00000636413.1:c.416C>T	ENSP00000490508.1:p.Ala139Val
ENST00000636471.1:c.752C>T	ENSP00000490317.1:p.Ala251Val
ENST00000636732.2:c.*469C>T	ENSP00000490175.1:n.*469C>T
ENST00000636820.1:n.852C>T
ENST00000637045.1:c.416C>T	ENSP00000490141.1:p.Ala139Val
ENST00000637267.2:c.752C>T	ENSP00000490293.2:p.Ala251Val
ENST00000637304.1:c.416C>T	ENSP00000490872.1:p.Ala139Val
ENST00000638007.1:c.416C>T	ENSP00000490723.1:p.Ala139Val
ENST00000638087.1:c.416C>T	ENSP00000490673.1:p.Ala139Val
ENST00000638128.1:c.-26C>T	ENSP00000490934.1:n.-26C>T
ENST00000675069.1:c.-133-5121C>T	ENSP00000502467.1:n.-133-5121C>T
ENST00000303660.8:c.749C>T	ENSP00000302501.4:p.Ala250Val
ENST00000392861.6:c.836C>T	ENSP00000376601.3:p.Ala279Val
ENST00000409487.7:c.752C>T	ENSP00000386854.2:p.Ala251Val
ENST00000419938.5:c.491C>T	ENSP00000394777.2:p.Ala164Val
ENST00000427902.5:c.839C>T	ENSP00000395496.2:p.Ala280Val
ENST00000440875.5:c.737C>T	ENSP00000475553.2:p.Ala246Val
ENST00000539609.7:c.680C>T	ENSP00000443792.2:p.Ala227Val
ENST00000558170.6:c.752C>T	ENSP00000454157.1:p.Ala251Val
ENST00000627532.2:c.752C>T	ENSP00000487174.1:p.Ala251Val
NM_001171653.1:c.680C>T	NP_001165124.1:p.Ala227Val
NM_014795.3:c.752C>T	NP_055610.1:p.Ala251Val
XM_006712881.2:c.752C>T	XP_006712944.1:p.Ala251Val
XM_006712882.2:c.752C>T	XP_006712945.1:p.Ala251Val
XM_011512231.1:c.743C>T	XP_011510533.1:p.Ala248Val
XM_011512232.1:c.731C>T	XP_011510534.1:p.Ala244Val
NM_014795.4:c.752C>T MANE Select	NP_055610.1:p.Ala251Val
NM_001171653.2:c.680C>T	NP_001165124.1:p.Ala227Val