Canonical Allele Identifier: CA2573133272

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1526203
• ClinVar RCV Id: RCV002052223
• dbSNP Id: rs2149876640

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398807del , CM000664.2:g.144398807del	GRCh38
NC_000002.11:g.145156374del , CM000664.1:g.145156374del	GRCh37
NC_000002.10:g.144872844del	NCBI36
NG_016431.1:g.126589del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2233del	ENSP00000508434.1:n.*2233del
ENST00000440875.6:c.1607del	ENSP00000475553.3:p.Asn536ThrfsTer22
ENST00000627532.3:c.2384del MANE Select	ENSP00000487174.1:p.Asn795ThrfsTer22
ENST00000636026.2:c.2384del	ENSP00000490776.1:p.Asn795ThrfsTer22
ENST00000636179.1:n.2353del
ENST00000636413.1:c.2048del	ENSP00000490508.1:p.Asn683ThrfsTer22
ENST00000636471.1:c.2459del	ENSP00000490317.1:p.Asn820ThrfsTer22
ENST00000636732.2:c.*2101del	ENSP00000490175.1:n.*2101del
ENST00000636820.1:n.2484del
ENST00000637045.1:c.2048del	ENSP00000490141.1:p.Asn683ThrfsTer22
ENST00000637304.1:c.2048del	ENSP00000490872.1:p.Asn683ThrfsTer22
ENST00000638007.1:c.2048del	ENSP00000490723.1:p.Asn683ThrfsTer22
ENST00000638087.1:c.2048del	ENSP00000490673.1:p.Asn683ThrfsTer22
ENST00000638128.1:c.1607del	ENSP00000490934.1:p.Asn536ThrfsTer22
ENST00000675069.1:c.-86del	ENSP00000502467.1:n.-86del
ENST00000675145.1:n.2932del
ENST00000303660.8:c.2381del	ENSP00000302501.4:p.Asn794ThrfsTer22
ENST00000409487.7:c.2384del	ENSP00000386854.2:p.Asn795ThrfsTer22
ENST00000419938.5:c.655+2396del	ENSP00000394777.2:n.655+2396del
ENST00000440875.5:c.1167+734del	ENSP00000475553.2:n.1167+734del
ENST00000539609.7:c.2312del	ENSP00000443792.2:p.Asn771ThrfsTer22
ENST00000558170.6:c.2384del	ENSP00000454157.1:p.Asn795ThrfsTer22
ENST00000627532.2:c.2384del	ENSP00000487174.1:p.Asn795ThrfsTer22
NM_001171653.1:c.2312del	NP_001165124.1:p.Asn771ThrfsTer22
NM_014795.3:c.2384del	NP_055610.1:p.Asn795ThrfsTer22
XM_006712881.2:c.2384del	XP_006712944.1:p.Asn795ThrfsTer22
XM_006712882.2:c.2384del	XP_006712945.1:p.Asn795ThrfsTer22
XM_011512231.1:c.2375del	XP_011510533.1:p.Asn792ThrfsTer22
XM_011512232.1:c.2363del	XP_011510534.1:p.Asn788ThrfsTer22
NM_014795.4:c.2384del MANE Select	NP_055610.1:p.Asn795ThrfsTer22
NM_001171653.2:c.2312del	NP_001165124.1:p.Asn771ThrfsTer22