Canonical Allele Identifier: CA348708390

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156361C>T (hg19) ; chr2:g.144398794C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398794C>T , CM000664.2:g.144398794C>T	GRCh38
NC_000002.11:g.145156361C>T , CM000664.1:g.145156361C>T	GRCh37
NC_000002.10:g.144872831C>T	NCBI36
NG_016431.1:g.126598G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2242G>A	ENSP00000508434.1:n.*2242G>A
ENST00000440875.6:c.1616G>A	ENSP00000475553.3:p.Ser539Asn
ENST00000627532.3:c.2393G>A MANE Select	ENSP00000487174.1:p.Ser798Asn
ENST00000636026.2:c.2393G>A	ENSP00000490776.1:p.Ser798Asn
ENST00000636179.1:n.2362G>A
ENST00000636413.1:c.2057G>A	ENSP00000490508.1:p.Ser686Asn
ENST00000636471.1:c.2468G>A	ENSP00000490317.1:p.Ser823Asn
ENST00000636732.2:c.*2110G>A	ENSP00000490175.1:n.*2110G>A
ENST00000636820.1:n.2493G>A
ENST00000637045.1:c.2057G>A	ENSP00000490141.1:p.Ser686Asn
ENST00000637304.1:c.2057G>A	ENSP00000490872.1:p.Ser686Asn
ENST00000638007.1:c.2057G>A	ENSP00000490723.1:p.Ser686Asn
ENST00000638087.1:c.2057G>A	ENSP00000490673.1:p.Ser686Asn
ENST00000638128.1:c.1616G>A	ENSP00000490934.1:p.Ser539Asn
ENST00000675069.1:c.-77G>A	ENSP00000502467.1:n.-77G>A
ENST00000675145.1:n.2941G>A
ENST00000303660.8:c.2390G>A	ENSP00000302501.4:p.Ser797Asn
ENST00000409487.7:c.2393G>A	ENSP00000386854.2:p.Ser798Asn
ENST00000419938.5:c.655+2405G>A	ENSP00000394777.2:n.655+2405G>A
ENST00000440875.5:c.1167+743G>A	ENSP00000475553.2:n.1167+743G>A
ENST00000539609.7:c.2321G>A	ENSP00000443792.2:p.Ser774Asn
ENST00000558170.6:c.2393G>A	ENSP00000454157.1:p.Ser798Asn
ENST00000627532.2:c.2393G>A	ENSP00000487174.1:p.Ser798Asn
NM_001171653.1:c.2321G>A	NP_001165124.1:p.Ser774Asn
NM_014795.3:c.2393G>A	NP_055610.1:p.Ser798Asn
XM_006712881.2:c.2393G>A	XP_006712944.1:p.Ser798Asn
XM_006712882.2:c.2393G>A	XP_006712945.1:p.Ser798Asn
XM_011512231.1:c.2384G>A	XP_011510533.1:p.Ser795Asn
XM_011512232.1:c.2372G>A	XP_011510534.1:p.Ser791Asn
NM_014795.4:c.2393G>A MANE Select	NP_055610.1:p.Ser798Asn
NM_001171653.2:c.2321G>A	NP_001165124.1:p.Ser774Asn