Canonical Allele Identifier: CA348708391

Gene: ZEB2

Linked Data

• COSMIC: COSM6087846
• MyVariant Identifiers: chr2:g.145156362T>A (hg19) ; chr2:g.144398795T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398795T>A , CM000664.2:g.144398795T>A	GRCh38
NC_000002.11:g.145156362T>A , CM000664.1:g.145156362T>A	GRCh37
NC_000002.10:g.144872832T>A	NCBI36
NG_016431.1:g.126597A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2241A>T	ENSP00000508434.1:n.*2241A>T
ENST00000440875.6:c.1615A>T	ENSP00000475553.3:p.Ser539Cys
ENST00000627532.3:c.2392A>T MANE Select	ENSP00000487174.1:p.Ser798Cys
ENST00000636026.2:c.2392A>T	ENSP00000490776.1:p.Ser798Cys
ENST00000636179.1:n.2361A>T
ENST00000636413.1:c.2056A>T	ENSP00000490508.1:p.Ser686Cys
ENST00000636471.1:c.2467A>T	ENSP00000490317.1:p.Ser823Cys
ENST00000636732.2:c.*2109A>T	ENSP00000490175.1:n.*2109A>T
ENST00000636820.1:n.2492A>T
ENST00000637045.1:c.2056A>T	ENSP00000490141.1:p.Ser686Cys
ENST00000637304.1:c.2056A>T	ENSP00000490872.1:p.Ser686Cys
ENST00000638007.1:c.2056A>T	ENSP00000490723.1:p.Ser686Cys
ENST00000638087.1:c.2056A>T	ENSP00000490673.1:p.Ser686Cys
ENST00000638128.1:c.1615A>T	ENSP00000490934.1:p.Ser539Cys
ENST00000675069.1:c.-78A>T	ENSP00000502467.1:n.-78A>T
ENST00000675145.1:n.2940A>T
ENST00000303660.8:c.2389A>T	ENSP00000302501.4:p.Ser797Cys
ENST00000409487.7:c.2392A>T	ENSP00000386854.2:p.Ser798Cys
ENST00000419938.5:c.655+2404A>T	ENSP00000394777.2:n.655+2404A>T
ENST00000440875.5:c.1167+742A>T	ENSP00000475553.2:n.1167+742A>T
ENST00000539609.7:c.2320A>T	ENSP00000443792.2:p.Ser774Cys
ENST00000558170.6:c.2392A>T	ENSP00000454157.1:p.Ser798Cys
ENST00000627532.2:c.2392A>T	ENSP00000487174.1:p.Ser798Cys
NM_001171653.1:c.2320A>T	NP_001165124.1:p.Ser774Cys
NM_014795.3:c.2392A>T	NP_055610.1:p.Ser798Cys
XM_006712881.2:c.2392A>T	XP_006712944.1:p.Ser798Cys
XM_006712882.2:c.2392A>T	XP_006712945.1:p.Ser798Cys
XM_011512231.1:c.2383A>T	XP_011510533.1:p.Ser795Cys
XM_011512232.1:c.2371A>T	XP_011510534.1:p.Ser791Cys
NM_014795.4:c.2392A>T MANE Select	NP_055610.1:p.Ser798Cys
NM_001171653.2:c.2320A>T	NP_001165124.1:p.Ser774Cys