Canonical Allele Identifier: CA348714735

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145161566A>T (hg19) ; chr2:g.144403999A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403999A>T , CM000664.2:g.144403999A>T	GRCh38
NC_000002.11:g.145161566A>T , CM000664.1:g.145161566A>T	GRCh37
NC_000002.10:g.144878036A>T	NCBI36
NG_016431.1:g.121393T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*573T>A	ENSP00000508434.1:n.*573T>A
ENST00000440875.6:c.-54T>A	ENSP00000475553.3:n.-54T>A
ENST00000627532.3:c.724T>A MANE Select	ENSP00000487174.1:p.Ser242Thr
ENST00000636026.2:c.724T>A	ENSP00000490776.1:p.Ser242Thr
ENST00000636179.1:n.693T>A
ENST00000636413.1:c.388T>A	ENSP00000490508.1:p.Ser130Thr
ENST00000636471.1:c.724T>A	ENSP00000490317.1:p.Ser242Thr
ENST00000636732.2:c.*441T>A	ENSP00000490175.1:n.*441T>A
ENST00000636820.1:n.824T>A
ENST00000637045.1:c.388T>A	ENSP00000490141.1:p.Ser130Thr
ENST00000637267.2:c.724T>A	ENSP00000490293.2:p.Ser242Thr
ENST00000637304.1:c.388T>A	ENSP00000490872.1:p.Ser130Thr
ENST00000638007.1:c.388T>A	ENSP00000490723.1:p.Ser130Thr
ENST00000638087.1:c.388T>A	ENSP00000490673.1:p.Ser130Thr
ENST00000638128.1:c.-54T>A	ENSP00000490934.1:n.-54T>A
ENST00000675069.1:c.-133-5149T>A	ENSP00000502467.1:n.-133-5149T>A
ENST00000303660.8:c.721T>A	ENSP00000302501.4:p.Ser241Thr
ENST00000392861.6:c.808T>A	ENSP00000376601.3:p.Ser270Thr
ENST00000409487.7:c.724T>A	ENSP00000386854.2:p.Ser242Thr
ENST00000419938.5:c.463T>A	ENSP00000394777.2:p.Ser155Thr
ENST00000427902.5:c.811T>A	ENSP00000395496.2:p.Ser271Thr
ENST00000440875.5:c.709T>A	ENSP00000475553.2:p.Ser237Thr
ENST00000497268.1:n.670T>A
ENST00000539609.7:c.652T>A	ENSP00000443792.2:p.Ser218Thr
ENST00000558170.6:c.724T>A	ENSP00000454157.1:p.Ser242Thr
ENST00000627532.2:c.724T>A	ENSP00000487174.1:p.Ser242Thr
NM_001171653.1:c.652T>A	NP_001165124.1:p.Ser218Thr
NM_014795.3:c.724T>A	NP_055610.1:p.Ser242Thr
XM_006712881.2:c.724T>A	XP_006712944.1:p.Ser242Thr
XM_006712882.2:c.724T>A	XP_006712945.1:p.Ser242Thr
XM_011512231.1:c.715T>A	XP_011510533.1:p.Ser239Thr
XM_011512232.1:c.703T>A	XP_011510534.1:p.Ser235Thr
NM_014795.4:c.724T>A MANE Select	NP_055610.1:p.Ser242Thr
NM_001171653.2:c.652T>A	NP_001165124.1:p.Ser218Thr