Canonical Allele Identifier: CA348714741

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161569A>C (hg19) ; chr2:g.144404002A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144404002A>C , CM000664.2:g.144404002A>C	GRCh38
NC_000002.11:g.145161569A>C , CM000664.1:g.145161569A>C	GRCh37
NC_000002.10:g.144878039A>C	NCBI36
NG_016431.1:g.121390T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*570T>G	ENSP00000508434.1:n.*570T>G
ENST00000440875.6:c.-57T>G	ENSP00000475553.3:n.-57T>G
ENST00000627532.3:c.721T>G MANE Select	ENSP00000487174.1:p.Phe241Val
ENST00000636026.2:c.721T>G	ENSP00000490776.1:p.Phe241Val
ENST00000636179.1:n.690T>G
ENST00000636413.1:c.385T>G	ENSP00000490508.1:p.Phe129Val
ENST00000636471.1:c.721T>G	ENSP00000490317.1:p.Phe241Val
ENST00000636732.2:c.*438T>G	ENSP00000490175.1:n.*438T>G
ENST00000636820.1:n.821T>G
ENST00000637045.1:c.385T>G	ENSP00000490141.1:p.Phe129Val
ENST00000637267.2:c.721T>G	ENSP00000490293.2:p.Phe241Val
ENST00000637304.1:c.385T>G	ENSP00000490872.1:p.Phe129Val
ENST00000638007.1:c.385T>G	ENSP00000490723.1:p.Phe129Val
ENST00000638087.1:c.385T>G	ENSP00000490673.1:p.Phe129Val
ENST00000638128.1:c.-57T>G	ENSP00000490934.1:n.-57T>G
ENST00000675069.1:c.-133-5152T>G	ENSP00000502467.1:n.-133-5152T>G
ENST00000303660.8:c.718T>G	ENSP00000302501.4:p.Phe240Val
ENST00000392861.6:c.805T>G	ENSP00000376601.3:p.Phe269Val
ENST00000409487.7:c.721T>G	ENSP00000386854.2:p.Phe241Val
ENST00000419938.5:c.460T>G	ENSP00000394777.2:p.Phe154Val
ENST00000427902.5:c.808T>G	ENSP00000395496.2:p.Phe270Val
ENST00000440875.5:c.706T>G	ENSP00000475553.2:p.Phe236Val
ENST00000497268.1:n.667T>G
ENST00000539609.7:c.649T>G	ENSP00000443792.2:p.Phe217Val
ENST00000558170.6:c.721T>G	ENSP00000454157.1:p.Phe241Val
ENST00000627532.2:c.721T>G	ENSP00000487174.1:p.Phe241Val
NM_001171653.1:c.649T>G	NP_001165124.1:p.Phe217Val
NM_014795.3:c.721T>G	NP_055610.1:p.Phe241Val
XM_006712881.2:c.721T>G	XP_006712944.1:p.Phe241Val
XM_006712882.2:c.721T>G	XP_006712945.1:p.Phe241Val
XM_011512231.1:c.712T>G	XP_011510533.1:p.Phe238Val
XM_011512232.1:c.700T>G	XP_011510534.1:p.Phe234Val
NM_014795.4:c.721T>G MANE Select	NP_055610.1:p.Phe241Val
NM_001171653.2:c.649T>G	NP_001165124.1:p.Phe217Val