Canonical Allele Identifier: CA16610153
Gene: ZEB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405331
ClinVar RCV Id: RCV000477195
dbSNP Id: rs1060500653
MyVariant Identifiers: chr2:g.145147568del (hg19) chr2:g.144390001del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.144390001del , CM000664.2:g.144390001del GRCh38
NC_000002.11:g.145147568del , CM000664.1:g.145147568del GRCh37
NC_000002.10:g.144864038del NCBI36
NG_016431.1:g.135391del

Transcript Alleles

HGVS Amino-acid change
ENST00000689298.1:c.*2944del ENSP00000508434.1:n.*2944del
ENST00000440875.6:c.2318del ENSP00000475553.3:p.Cys773LeufsTer?
ENST00000627532.3:c.3095del MANE Select ENSP00000487174.1:p.Cys1032LeufsTer?
ENST00000636026.2:c.3095del ENSP00000490776.1:p.Cys1032LeufsTer?
ENST00000636179.1:n.3064del
ENST00000636413.1:c.2759del ENSP00000490508.1:p.Cys920LeufsTer?
ENST00000636471.1:c.3170del ENSP00000490317.1:p.Cys1057LeufsTer?
ENST00000636732.2:c.*2812del ENSP00000490175.1:n.*2812del
ENST00000636820.1:n.3195del
ENST00000637045.1:c.2759del ENSP00000490141.1:p.Cys920LeufsTer?
ENST00000637304.1:c.2759del ENSP00000490872.1:p.Cys920LeufsTer?
ENST00000638007.1:c.2759del ENSP00000490723.1:p.Cys920LeufsTer?
ENST00000638087.1:c.2759del ENSP00000490673.1:p.Cys920LeufsTer?
ENST00000638128.1:c.2318del ENSP00000490934.1:p.Cys773LeufsTer?
ENST00000639389.1:c.151+6411del ENSP00000492572.1:n.151+6411del
ENST00000647488.1:c.315del ENSP00000494820.1:n.315del
ENST00000675069.1:c.626del ENSP00000502467.1:p.Cys209LeufsTer?
ENST00000303660.8:c.3092del ENSP00000302501.4:p.Cys1031LeufsTer?
ENST00000409487.7:c.3095del ENSP00000386854.2:p.Cys1032LeufsTer?
ENST00000419938.5:c.656-1119del ENSP00000394777.2:n.656-1119del
ENST00000539609.7:c.3023del ENSP00000443792.2:p.Cys1008LeufsTer?
ENST00000558170.6:c.3095del ENSP00000454157.1:p.Cys1032LeufsTer?
ENST00000627532.2:c.3095del ENSP00000487174.1:p.Cys1032LeufsTer?
NM_001171653.1:c.3023del NP_001165124.1:p.Cys1008LeufsTer?
NM_014795.3:c.3095del NP_055610.1:p.Cys1032LeufsTer?
XM_006712881.2:c.3095del XP_006712944.1:p.Cys1032LeufsTer?
XM_006712882.2:c.3095del XP_006712945.1:p.Cys1032LeufsTer?
XM_011512231.1:c.3086del XP_011510533.1:p.Cys1029LeufsTer?
XM_011512232.1:c.3074del XP_011510534.1:p.Cys1025LeufsTer?
NM_014795.4:c.3095del MANE Select NP_055610.1:p.Cys1032LeufsTer?
NM_001171653.2:c.3023del NP_001165124.1:p.Cys1008LeufsTer?
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