Canonical Allele Identifier: CA297632

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 181755
• ClinVar RCV Id: RCV000159495
• dbSNP Id: rs730881212
• MyVariant Identifiers: chr2:g.145154044del (hg19) ; chr2:g.144396477del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144396477del , CM000664.2:g.144396477del	GRCh38
NC_000002.11:g.145154044del , CM000664.1:g.145154044del	GRCh37
NC_000002.10:g.144870514del	NCBI36
NG_016431.1:g.128915del

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*2851del	ENSP00000508434.1:n.*2851del
ENST00000440875.6:c.2225del	ENSP00000475553.3:p.Cys742LeufsTer?
ENST00000627532.3:c.3002del MANE Select	ENSP00000487174.1:p.Cys1001LeufsTer?
ENST00000636026.2:c.3002del	ENSP00000490776.1:p.Cys1001LeufsTer?
ENST00000636179.1:n.2971del
ENST00000636413.1:c.2666del	ENSP00000490508.1:p.Cys889LeufsTer?
ENST00000636471.1:c.3077del	ENSP00000490317.1:p.Cys1026LeufsTer?
ENST00000636732.2:c.*2719del	ENSP00000490175.1:n.*2719del
ENST00000636820.1:n.3102del
ENST00000637045.1:c.2666del	ENSP00000490141.1:p.Cys889LeufsTer?
ENST00000637304.1:c.2666del	ENSP00000490872.1:p.Cys889LeufsTer?
ENST00000638007.1:c.2666del	ENSP00000490723.1:p.Cys889LeufsTer?
ENST00000638087.1:c.2666del	ENSP00000490673.1:p.Cys889LeufsTer?
ENST00000638128.1:c.2225del	ENSP00000490934.1:p.Cys742LeufsTer?
ENST00000639389.1:c.86del	ENSP00000492572.1:p.Cys29LeufsTer?
ENST00000647488.1:c.134del	ENSP00000494820.1:p.Cys45LeufsTer25
ENST00000675069.1:c.533del	ENSP00000502467.1:p.Cys178LeufsTer?
ENST00000303660.8:c.2999del	ENSP00000302501.4:p.Cys1000LeufsTer?
ENST00000409487.7:c.3002del	ENSP00000386854.2:p.Cys1001LeufsTer?
ENST00000419938.5:c.655+4722del	ENSP00000394777.2:n.655+4722del
ENST00000539609.7:c.2930del	ENSP00000443792.2:p.Cys977LeufsTer?
ENST00000558170.6:c.3002del	ENSP00000454157.1:p.Cys1001LeufsTer?
ENST00000627532.2:c.3002del	ENSP00000487174.1:p.Cys1001LeufsTer?
NM_001171653.1:c.2930del	NP_001165124.1:p.Cys977LeufsTer?
NM_014795.3:c.3002del	NP_055610.1:p.Cys1001LeufsTer?
XM_006712881.2:c.3002del	XP_006712944.1:p.Cys1001LeufsTer?
XM_006712882.2:c.3002del	XP_006712945.1:p.Cys1001LeufsTer?
XM_011512231.1:c.2993del	XP_011510533.1:p.Cys998LeufsTer?
XM_011512232.1:c.2981del	XP_011510534.1:p.Cys994LeufsTer?
NM_014795.4:c.3002del MANE Select	NP_055610.1:p.Cys1001LeufsTer?
NM_001171653.2:c.2930del	NP_001165124.1:p.Cys977LeufsTer?