Canonical Allele Identifier: CA916082205

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 869448
• ClinVar RCV Id: RCV001089543
• dbSNP Id: rs1703267358

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398885del , CM000664.2:g.144398885del	GRCh38
NC_000002.11:g.145156452del , CM000664.1:g.145156452del	GRCh37
NC_000002.10:g.144872922del	NCBI36
NG_016431.1:g.126508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2152del	ENSP00000508434.1:n.*2152del
ENST00000440875.6:c.1526del	ENSP00000475553.3:p.Asn509IlefsTer19
ENST00000627532.3:c.2303del MANE Select	ENSP00000487174.1:p.Asn768IlefsTer19
ENST00000636026.2:c.2303del	ENSP00000490776.1:p.Asn768IlefsTer19
ENST00000636179.1:n.2272del
ENST00000636413.1:c.1967del	ENSP00000490508.1:p.Asn656IlefsTer19
ENST00000636471.1:c.2378del	ENSP00000490317.1:p.Asn793IlefsTer19
ENST00000636732.2:c.*2020del	ENSP00000490175.1:n.*2020del
ENST00000636820.1:n.2403del
ENST00000637045.1:c.1967del	ENSP00000490141.1:p.Asn656IlefsTer19
ENST00000637304.1:c.1967del	ENSP00000490872.1:p.Asn656IlefsTer19
ENST00000638007.1:c.1967del	ENSP00000490723.1:p.Asn656IlefsTer19
ENST00000638087.1:c.1967del	ENSP00000490673.1:p.Asn656IlefsTer19
ENST00000638128.1:c.1526del	ENSP00000490934.1:p.Asn509IlefsTer19
ENST00000675069.1:c.-133-34del	ENSP00000502467.1:n.-133-34del
ENST00000675145.1:n.2851del
ENST00000303660.8:c.2300del	ENSP00000302501.4:p.Asn767IlefsTer19
ENST00000409487.7:c.2303del	ENSP00000386854.2:p.Asn768IlefsTer19
ENST00000419938.5:c.655+2315del	ENSP00000394777.2:n.655+2315del
ENST00000440875.5:c.1167+653del	ENSP00000475553.2:n.1167+653del
ENST00000539609.7:c.2231del	ENSP00000443792.2:p.Asn744IlefsTer19
ENST00000558170.6:c.2303del	ENSP00000454157.1:p.Asn768IlefsTer19
ENST00000627532.2:c.2303del	ENSP00000487174.1:p.Asn768IlefsTer19
NM_001171653.1:c.2231del	NP_001165124.1:p.Asn744IlefsTer19
NM_014795.3:c.2303del	NP_055610.1:p.Asn768IlefsTer19
XM_006712881.2:c.2303del	XP_006712944.1:p.Asn768IlefsTer19
XM_006712882.2:c.2303del	XP_006712945.1:p.Asn768IlefsTer19
XM_011512231.1:c.2294del	XP_011510533.1:p.Asn765IlefsTer19
XM_011512232.1:c.2282del	XP_011510534.1:p.Asn761IlefsTer19
NM_014795.4:c.2303del MANE Select	NP_055610.1:p.Asn768IlefsTer19
NM_001171653.2:c.2231del	NP_001165124.1:p.Asn744IlefsTer19