Canonical Allele Identifier: CA658795852

Gene: ZEB2

Linked Data

• ClinVar Variation Id: 498049
• ClinVar RCV Id: RCV000595163
• dbSNP Id: rs1553962048
• MyVariant Identifiers: chr2:g.145161500_145161501del (hg19) ; chr2:g.144403933_144403934del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.144403938_144403939del , CM000664.2:g.144403938_144403939del	GRCh38
NC_000002.11:g.145161505_145161506del , CM000664.1:g.145161505_145161506del	GRCh37
NC_000002.10:g.144877975_144877976del	NCBI36
NG_016431.1:g.121458_121459del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000689298.1:c.*638_*639del	ENSP00000508434.1:n.*638_*639del
ENST00000440875.6:c.12_13del	ENSP00000475553.3:p.His4GlnfsTer16
ENST00000627532.3:c.789_790del MANE Select	ENSP00000487174.1:p.His263GlnfsTer16
ENST00000636026.2:c.789_790del	ENSP00000490776.1:p.His263GlnfsTer16
ENST00000636179.1:n.758_759del
ENST00000636413.1:c.453_454del	ENSP00000490508.1:p.His151GlnfsTer16
ENST00000636471.1:c.789_790del	ENSP00000490317.1:p.His263GlnfsTer16
ENST00000636732.2:c.*506_*507del	ENSP00000490175.1:n.*506_*507del
ENST00000636820.1:n.889_890del
ENST00000637045.1:c.453_454del	ENSP00000490141.1:p.His151GlnfsTer16
ENST00000637267.2:c.789_790del	ENSP00000490293.2:p.His263GlnfsTer16
ENST00000637304.1:c.453_454del	ENSP00000490872.1:p.His151GlnfsTer16
ENST00000638007.1:c.453_454del	ENSP00000490723.1:p.His151GlnfsTer16
ENST00000638087.1:c.453_454del	ENSP00000490673.1:p.His151GlnfsTer16
ENST00000638128.1:c.12_13del	ENSP00000490934.1:p.His4GlnfsTer16
ENST00000675069.1:c.-133-5084_-133-5083del	ENSP00000502467.1:n.-133-5084_-133-5083del
ENST00000303660.8:c.786_787del	ENSP00000302501.4:p.His262GlnfsTer16
ENST00000392861.6:c.873_874del	ENSP00000376601.3:p.His291GlnfsTer16
ENST00000409487.7:c.789_790del	ENSP00000386854.2:p.His263GlnfsTer16
ENST00000419938.5:c.528_529del	ENSP00000394777.2:p.His176GlnfsTer16
ENST00000427902.5:c.876_877del	ENSP00000395496.2:p.His292GlnfsTer16
ENST00000440875.5:c.774_775del	ENSP00000475553.2:p.His258GlnfsTer16
ENST00000539609.7:c.717_718del	ENSP00000443792.2:p.His239GlnfsTer16
ENST00000558170.6:c.789_790del	ENSP00000454157.1:p.His263GlnfsTer16
ENST00000627532.2:c.789_790del	ENSP00000487174.1:p.His263GlnfsTer16
NM_001171653.1:c.717_718del	NP_001165124.1:p.His239GlnfsTer16
NM_014795.3:c.789_790del	NP_055610.1:p.His263GlnfsTer16
XM_006712881.2:c.789_790del	XP_006712944.1:p.His263GlnfsTer16
XM_006712882.2:c.789_790del	XP_006712945.1:p.His263GlnfsTer16
XM_011512231.1:c.780_781del	XP_011510533.1:p.His260GlnfsTer16
XM_011512232.1:c.768_769del	XP_011510534.1:p.His256GlnfsTer16
NM_014795.4:c.789_790del MANE Select	NP_055610.1:p.His263GlnfsTer16
NM_001171653.2:c.717_718del	NP_001165124.1:p.His239GlnfsTer16