Canonical Allele Identifier: CA348708321

Gene: ZEB2

Linked Data

• MyVariant Identifiers: chr2:g.145156332A>T (hg19) ; chr2:g.144398765A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398765A>T , CM000664.2:g.144398765A>T	GRCh38
NC_000002.11:g.145156332A>T , CM000664.1:g.145156332A>T	GRCh37
NC_000002.10:g.144872802A>T	NCBI36
NG_016431.1:g.126627T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2271T>A	ENSP00000508434.1:n.*2271T>A
ENST00000440875.6:c.1645T>A	ENSP00000475553.3:p.Ser549Thr
ENST00000627532.3:c.2422T>A MANE Select	ENSP00000487174.1:p.Ser808Thr
ENST00000636026.2:c.2422T>A	ENSP00000490776.1:p.Ser808Thr
ENST00000636179.1:n.2391T>A
ENST00000636413.1:c.2086T>A	ENSP00000490508.1:p.Ser696Thr
ENST00000636471.1:c.2497T>A	ENSP00000490317.1:p.Ser833Thr
ENST00000636732.2:c.*2139T>A	ENSP00000490175.1:n.*2139T>A
ENST00000636820.1:n.2522T>A
ENST00000637045.1:c.2086T>A	ENSP00000490141.1:p.Ser696Thr
ENST00000637304.1:c.2086T>A	ENSP00000490872.1:p.Ser696Thr
ENST00000638007.1:c.2086T>A	ENSP00000490723.1:p.Ser696Thr
ENST00000638087.1:c.2086T>A	ENSP00000490673.1:p.Ser696Thr
ENST00000638128.1:c.1645T>A	ENSP00000490934.1:p.Ser549Thr
ENST00000675069.1:c.-48T>A	ENSP00000502467.1:n.-48T>A
ENST00000675145.1:n.2970T>A
ENST00000303660.8:c.2419T>A	ENSP00000302501.4:p.Ser807Thr
ENST00000409487.7:c.2422T>A	ENSP00000386854.2:p.Ser808Thr
ENST00000419938.5:c.655+2434T>A	ENSP00000394777.2:n.655+2434T>A
ENST00000440875.5:c.1167+772T>A	ENSP00000475553.2:n.1167+772T>A
ENST00000539609.7:c.2350T>A	ENSP00000443792.2:p.Ser784Thr
ENST00000558170.6:c.2422T>A	ENSP00000454157.1:p.Ser808Thr
ENST00000627532.2:c.2422T>A	ENSP00000487174.1:p.Ser808Thr
NM_001171653.1:c.2350T>A	NP_001165124.1:p.Ser784Thr
NM_014795.3:c.2422T>A	NP_055610.1:p.Ser808Thr
XM_006712881.2:c.2422T>A	XP_006712944.1:p.Ser808Thr
XM_006712882.2:c.2422T>A	XP_006712945.1:p.Ser808Thr
XM_011512231.1:c.2413T>A	XP_011510533.1:p.Ser805Thr
XM_011512232.1:c.2401T>A	XP_011510534.1:p.Ser801Thr
NM_014795.4:c.2422T>A MANE Select	NP_055610.1:p.Ser808Thr
NM_001171653.2:c.2350T>A	NP_001165124.1:p.Ser784Thr