Canonical Allele Identifier: CA658657064

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 451579
• ClinVar RCV Id: RCV000522940
• dbSNP Id: rs587776605
• MyVariant Identifiers: chr2:g.145161529_145161530del (hg19) ; chr2:g.144403962_144403963del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403963_144403964del , CM000664.2:g.144403963_144403964del	GRCh38
NC_000002.11:g.145161530_145161531del , CM000664.1:g.145161530_145161531del	GRCh37
NC_000002.10:g.144878000_144878001del	NCBI36
NG_016431.1:g.121429_121430del

Transcript Alleles

HGVS	Amino-acid change
ENST00000689298.1:c.*609_*610del	ENSP00000508434.1:n.*609_*610del
ENST00000440875.6:c.-18_-17del	ENSP00000475553.3:n.-18_-17del
ENST00000627532.3:c.760_761del MANE Select	ENSP00000487174.1:p.Thr254ProfsTer25
ENST00000636026.2:c.760_761del	ENSP00000490776.1:p.Thr254ProfsTer25
ENST00000636179.1:n.729_730del
ENST00000636413.1:c.424_425del	ENSP00000490508.1:p.Thr142ProfsTer25
ENST00000636471.1:c.760_761del	ENSP00000490317.1:p.Thr254ProfsTer25
ENST00000636732.2:c.*477_*478del	ENSP00000490175.1:n.*477_*478del
ENST00000636820.1:n.860_861del
ENST00000637045.1:c.424_425del	ENSP00000490141.1:p.Thr142ProfsTer25
ENST00000637267.2:c.760_761del	ENSP00000490293.2:p.Thr254ProfsTer25
ENST00000637304.1:c.424_425del	ENSP00000490872.1:p.Thr142ProfsTer25
ENST00000638007.1:c.424_425del	ENSP00000490723.1:p.Thr142ProfsTer25
ENST00000638087.1:c.424_425del	ENSP00000490673.1:p.Thr142ProfsTer25
ENST00000638128.1:c.-18_-17del	ENSP00000490934.1:n.-18_-17del
ENST00000675069.1:c.-133-5113_-133-5112del	ENSP00000502467.1:n.-133-5113_-133-5112de...
ENST00000303660.8:c.757_758del	ENSP00000302501.4:p.Thr253ProfsTer25
ENST00000392861.6:c.844_845del	ENSP00000376601.3:p.Thr282ProfsTer25
ENST00000409487.7:c.760_761del	ENSP00000386854.2:p.Thr254ProfsTer25
ENST00000419938.5:c.499_500del	ENSP00000394777.2:p.Thr167ProfsTer25
ENST00000427902.5:c.847_848del	ENSP00000395496.2:p.Thr283ProfsTer25
ENST00000440875.5:c.745_746del	ENSP00000475553.2:p.Thr249ProfsTer25
ENST00000539609.7:c.688_689del	ENSP00000443792.2:p.Thr230ProfsTer25
ENST00000558170.6:c.760_761del	ENSP00000454157.1:p.Thr254ProfsTer25
ENST00000627532.2:c.760_761del	ENSP00000487174.1:p.Thr254ProfsTer25
NM_001171653.1:c.688_689del	NP_001165124.1:p.Thr230ProfsTer25
NM_014795.3:c.760_761del	NP_055610.1:p.Thr254ProfsTer25
XM_006712881.2:c.760_761del	XP_006712944.1:p.Thr254ProfsTer25
XM_006712882.2:c.760_761del	XP_006712945.1:p.Thr254ProfsTer25
XM_011512231.1:c.751_752del	XP_011510533.1:p.Thr251ProfsTer25
XM_011512232.1:c.739_740del	XP_011510534.1:p.Thr247ProfsTer25
NM_014795.4:c.760_761del MANE Select	NP_055610.1:p.Thr254ProfsTer25
NM_001171653.2:c.688_689del	NP_001165124.1:p.Thr230ProfsTer25