Canonical Allele Identifier: CA658795858

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 534632
• ClinVar RCV Id: RCV000642253
• dbSNP Id: rs1553961487
• MyVariant Identifiers: chr2:g.145155948del (hg19) ; chr2:g.144398381del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144398382del , CM000664.2:g.144398382del	GRCh38
NC_000002.11:g.145155949del , CM000664.1:g.145155949del	GRCh37
NC_000002.10:g.144872419del	NCBI36
NG_016431.1:g.127011del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*2655del	ENSP00000508434.1:n.*2655del
ENST00000440875.6:c.2029del	ENSP00000475553.3:p.Ala677ProfsTer?
ENST00000627532.3:c.2806del MANE Select	ENSP00000487174.1:p.Ala936ProfsTer?
ENST00000636026.2:c.2806del	ENSP00000490776.1:p.Ala936ProfsTer?
ENST00000636179.1:n.2775del
ENST00000636413.1:c.2470del	ENSP00000490508.1:p.Ala824ProfsTer?
ENST00000636471.1:c.2881del	ENSP00000490317.1:p.Ala961ProfsTer?
ENST00000636732.2:c.*2523del	ENSP00000490175.1:n.*2523del
ENST00000636820.1:n.2906del
ENST00000637045.1:c.2470del	ENSP00000490141.1:p.Ala824ProfsTer?
ENST00000637304.1:c.2470del	ENSP00000490872.1:p.Ala824ProfsTer?
ENST00000638007.1:c.2470del	ENSP00000490723.1:p.Ala824ProfsTer?
ENST00000638087.1:c.2470del	ENSP00000490673.1:p.Ala824ProfsTer?
ENST00000638128.1:c.2029del	ENSP00000490934.1:p.Ala677ProfsTer?
ENST00000675069.1:c.337del	ENSP00000502467.1:p.Ala113ProfsTer?
ENST00000303660.8:c.2803del	ENSP00000302501.4:p.Ala935ProfsTer?
ENST00000409487.7:c.2806del	ENSP00000386854.2:p.Ala936ProfsTer?
ENST00000419938.5:c.655+2818del	ENSP00000394777.2:n.655+2818del
ENST00000440875.5:c.1168-453del	ENSP00000475553.2:n.1168-453del
ENST00000539609.7:c.2734del	ENSP00000443792.2:p.Ala912ProfsTer?
ENST00000558170.6:c.2806del	ENSP00000454157.1:p.Ala936ProfsTer?
ENST00000627532.2:c.2806del	ENSP00000487174.1:p.Ala936ProfsTer?
NM_001171653.1:c.2734del	NP_001165124.1:p.Ala912ProfsTer?
NM_014795.3:c.2806del	NP_055610.1:p.Ala936ProfsTer?
XM_006712881.2:c.2806del	XP_006712944.1:p.Ala936ProfsTer?
XM_006712882.2:c.2806del	XP_006712945.1:p.Ala936ProfsTer?
XM_011512231.1:c.2797del	XP_011510533.1:p.Ala933ProfsTer?
XM_011512232.1:c.2785del	XP_011510534.1:p.Ala929ProfsTer?
NM_014795.4:c.2806del MANE Select	NP_055610.1:p.Ala936ProfsTer?
NM_001171653.2:c.2734del	NP_001165124.1:p.Ala912ProfsTer?