Canonical Allele Identifier: CA2573133279

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 1686311
• ClinVar RCV Id: RCV002246824
• dbSNP Id: rs2149877032

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144399339del , CM000664.2:g.144399339del	GRCh38
NC_000002.11:g.145156906del , CM000664.1:g.145156906del	GRCh37
NC_000002.10:g.144873376del	NCBI36
NG_016431.1:g.126053del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*1697del	ENSP00000508434.1:n.*1697del
ENST00000440875.6:c.1071del	ENSP00000475553.3:p.His358MetfsTer4
ENST00000627532.3:c.1848del MANE Select	ENSP00000487174.1:p.His617MetfsTer4
ENST00000636026.2:c.1848del	ENSP00000490776.1:p.His617MetfsTer4
ENST00000636179.1:n.1817del
ENST00000636413.1:c.1512del	ENSP00000490508.1:p.His505MetfsTer4
ENST00000636471.1:c.1923del	ENSP00000490317.1:p.His642MetfsTer4
ENST00000636732.2:c.*1565del	ENSP00000490175.1:n.*1565del
ENST00000636820.1:n.1948del
ENST00000637045.1:c.1512del	ENSP00000490141.1:p.His505MetfsTer4
ENST00000637304.1:c.1512del	ENSP00000490872.1:p.His505MetfsTer4
ENST00000638007.1:c.1512del	ENSP00000490723.1:p.His505MetfsTer4
ENST00000638087.1:c.1512del	ENSP00000490673.1:p.His505MetfsTer4
ENST00000638128.1:c.1071del	ENSP00000490934.1:p.His358MetfsTer4
ENST00000675069.1:c.-133-489del	ENSP00000502467.1:n.-133-489del
ENST00000675145.1:n.2396del
ENST00000303660.8:c.1845del	ENSP00000302501.4:p.His616MetfsTer4
ENST00000409487.7:c.1848del	ENSP00000386854.2:p.His617MetfsTer4
ENST00000419938.5:c.655+1860del	ENSP00000394777.2:n.655+1860del
ENST00000427902.5:c.1935del	ENSP00000395496.2:p.His646MetfsTer4
ENST00000440875.5:c.1167+198del	ENSP00000475553.2:n.1167+198del
ENST00000539609.7:c.1776del	ENSP00000443792.2:p.His593MetfsTer4
ENST00000558170.6:c.1848del	ENSP00000454157.1:p.His617MetfsTer4
ENST00000627532.2:c.1848del	ENSP00000487174.1:p.His617MetfsTer4
NM_001171653.1:c.1776del	NP_001165124.1:p.His593MetfsTer4
NM_014795.3:c.1848del	NP_055610.1:p.His617MetfsTer4
XM_006712881.2:c.1848del	XP_006712944.1:p.His617MetfsTer4
XM_006712882.2:c.1848del	XP_006712945.1:p.His617MetfsTer4
XM_011512231.1:c.1839del	XP_011510533.1:p.His614MetfsTer4
XM_011512232.1:c.1827del	XP_011510534.1:p.His610MetfsTer4
NM_014795.4:c.1848del MANE Select	NP_055610.1:p.His617MetfsTer4
NM_001171653.2:c.1776del	NP_001165124.1:p.His593MetfsTer4