Canonical Allele Identifier: CA2825000995

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 3067788
• ClinVar RCV Id: RCV003993477

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398759_144398774del , CM000664.2:g.144398759_144398774del	GRCh38
NC_000002.11:g.145156326_145156341del , CM000664.1:g.145156326_145156341del	GRCh37
NC_000002.10:g.144872796_144872811del	NCBI36
NG_016431.1:g.126622_126637del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2266_*2281del	ENSP00000508434.1:n.*2266_*2281del
ENST00000440875.6:c.1640_1655del	ENSP00000475553.3:p.Phe547SerfsTer6
ENST00000627532.3:c.2417_2432del MANE Select	ENSP00000487174.1:p.Phe806SerfsTer6
ENST00000636026.2:c.2417_2432del	ENSP00000490776.1:p.Phe806SerfsTer6
ENST00000636179.1:n.2386_2401del
ENST00000636413.1:c.2081_2096del	ENSP00000490508.1:p.Phe694SerfsTer6
ENST00000636471.1:c.2492_2507del	ENSP00000490317.1:p.Phe831SerfsTer6
ENST00000636732.2:c.*2134_*2149del	ENSP00000490175.1:n.*2134_*2149del
ENST00000636820.1:n.2517_2532del
ENST00000637045.1:c.2081_2096del	ENSP00000490141.1:p.Phe694SerfsTer6
ENST00000637304.1:c.2081_2096del	ENSP00000490872.1:p.Phe694SerfsTer6
ENST00000638007.1:c.2081_2096del	ENSP00000490723.1:p.Phe694SerfsTer6
ENST00000638087.1:c.2081_2096del	ENSP00000490673.1:p.Phe694SerfsTer6
ENST00000638128.1:c.1640_1655del	ENSP00000490934.1:p.Phe547SerfsTer6
ENST00000675069.1:c.-53_-38del	ENSP00000502467.1:n.-53_-38del
ENST00000675145.1:n.2965_2980del
ENST00000303660.8:c.2414_2429del	ENSP00000302501.4:p.Phe805SerfsTer6
ENST00000409487.7:c.2417_2432del	ENSP00000386854.2:p.Phe806SerfsTer6
ENST00000419938.5:c.655+2429_655+2444del	ENSP00000394777.2:n.655+2429_655+2444del
ENST00000440875.5:c.1167+767_1167+782del	ENSP00000475553.2:n.1167+767_1167+782del
ENST00000539609.7:c.2345_2360del	ENSP00000443792.2:p.Phe782SerfsTer6
ENST00000558170.6:c.2417_2432del	ENSP00000454157.1:p.Phe806SerfsTer6
ENST00000627532.2:c.2417_2432del	ENSP00000487174.1:p.Phe806SerfsTer6
NM_001171653.1:c.2345_2360del	NP_001165124.1:p.Phe782SerfsTer6
NM_014795.3:c.2417_2432del	NP_055610.1:p.Phe806SerfsTer6
XM_006712881.2:c.2417_2432del	XP_006712944.1:p.Phe806SerfsTer6
XM_006712882.2:c.2417_2432del	XP_006712945.1:p.Phe806SerfsTer6
XM_011512231.1:c.2408_2423del	XP_011510533.1:p.Phe803SerfsTer6
XM_011512232.1:c.2396_2411del	XP_011510534.1:p.Phe799SerfsTer6
NM_014795.4:c.2417_2432del MANE Select	NP_055610.1:p.Phe806SerfsTer6
NM_001171653.2:c.2345_2360del	NP_001165124.1:p.Phe782SerfsTer6