Canonical Allele Identifier: CA348714679

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161542A>C (hg19) ; chr2:g.144403975A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403975A>C , CM000664.2:g.144403975A>C	GRCh38
NC_000002.11:g.145161542A>C , CM000664.1:g.145161542A>C	GRCh37
NC_000002.10:g.144878012A>C	NCBI36
NG_016431.1:g.121417T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*597T>G	ENSP00000508434.1:n.*597T>G
ENST00000440875.6:c.-30T>G	ENSP00000475553.3:n.-30T>G
ENST00000627532.3:c.748T>G MANE Select	ENSP00000487174.1:p.Phe250Val
ENST00000636026.2:c.748T>G	ENSP00000490776.1:p.Phe250Val
ENST00000636179.1:n.717T>G
ENST00000636413.1:c.412T>G	ENSP00000490508.1:p.Phe138Val
ENST00000636471.1:c.748T>G	ENSP00000490317.1:p.Phe250Val
ENST00000636732.2:c.*465T>G	ENSP00000490175.1:n.*465T>G
ENST00000636820.1:n.848T>G
ENST00000637045.1:c.412T>G	ENSP00000490141.1:p.Phe138Val
ENST00000637267.2:c.748T>G	ENSP00000490293.2:p.Phe250Val
ENST00000637304.1:c.412T>G	ENSP00000490872.1:p.Phe138Val
ENST00000638007.1:c.412T>G	ENSP00000490723.1:p.Phe138Val
ENST00000638087.1:c.412T>G	ENSP00000490673.1:p.Phe138Val
ENST00000638128.1:c.-30T>G	ENSP00000490934.1:n.-30T>G
ENST00000675069.1:c.-133-5125T>G	ENSP00000502467.1:n.-133-5125T>G
ENST00000303660.8:c.745T>G	ENSP00000302501.4:p.Phe249Val
ENST00000392861.6:c.832T>G	ENSP00000376601.3:p.Phe278Val
ENST00000409487.7:c.748T>G	ENSP00000386854.2:p.Phe250Val
ENST00000419938.5:c.487T>G	ENSP00000394777.2:p.Phe163Val
ENST00000427902.5:c.835T>G	ENSP00000395496.2:p.Phe279Val
ENST00000440875.5:c.733T>G	ENSP00000475553.2:p.Phe245Val
ENST00000539609.7:c.676T>G	ENSP00000443792.2:p.Phe226Val
ENST00000558170.6:c.748T>G	ENSP00000454157.1:p.Phe250Val
ENST00000627532.2:c.748T>G	ENSP00000487174.1:p.Phe250Val
NM_001171653.1:c.676T>G	NP_001165124.1:p.Phe226Val
NM_014795.3:c.748T>G	NP_055610.1:p.Phe250Val
XM_006712881.2:c.748T>G	XP_006712944.1:p.Phe250Val
XM_006712882.2:c.748T>G	XP_006712945.1:p.Phe250Val
XM_011512231.1:c.739T>G	XP_011510533.1:p.Phe247Val
XM_011512232.1:c.727T>G	XP_011510534.1:p.Phe243Val
NM_014795.4:c.748T>G MANE Select	NP_055610.1:p.Phe250Val
NM_001171653.2:c.676T>G	NP_001165124.1:p.Phe226Val