Canonical Allele Identifier: CA624865065
Gene: WRAP53 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407531
ClinVar RCV Id: RCV001918493
dbSNP Id: rs1451505833

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.7688998_7689000del , CM000679.2:g.7688998_7689000del GRCh38
NC_000017.10:g.7592316_7592318del , CM000679.1:g.7592316_7592318del GRCh37
NC_000017.9:g.7533041_7533043del NCBI36
NG_017013.2:g.3558_3560del , LRG_321:g.3558_3560del
NG_028245.1:g.7928_7930del , LRG_375:g.7928_7930del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698742.1:c.350_352del ENSP00000513904.1:p.Glu117del
ENST00000698743.1:c.350_352del ENSP00000513905.1:p.Glu117del
ENST00000698744.1:c.350_352del ENSP00000513906.1:p.Glu117del
ENST00000698745.1:c.350_352del ENSP00000513907.1:p.Glu117del
ENST00000698746.1:c.350_352del ENSP00000513908.1:p.Glu117del
ENST00000396463.7:c.350_352del MANE Select ENSP00000379727.3:p.Glu117del
ENST00000316024.9:c.350_352del ENSP00000324203.5:p.Glu117del
ENST00000396463.6:c.350_352del ENSP00000379727.2:p.Glu117del
ENST00000431639.6:c.350_352del ENSP00000397219.2:p.Glu117del
ENST00000457584.6:c.350_352del ENSP00000411061.2:p.Glu117del
ENST00000467699.5:n.436_438del
ENST00000498311.5:c.350_352del ENSP00000432991.1:p.Glu117del
ENST00000534050.5:c.350_352del ENSP00000434999.1:p.Glu117del
NM_001143990.1:c.350_352del NP_001137462.1:p.Glu117del
NM_001143991.1:c.350_352del NP_001137463.1:p.Glu117del
NM_001143992.1:c.350_352del NP_001137464.1:p.Glu117del
NM_018081.2:c.350_352del , LRG_375t1:c.350_352del NP_060551.2:p.Glu117del
XM_011523952.2:c.-283_-281del XP_011522254.1:n.-283_-281del
XM_024450824.1:c.-1726_-1724del XP_024306592.1:n.-1726_-1724del
XM_024450825.1:c.350_352del XP_024306593.1:p.Glu117del
XR_001752551.2:n.595_597del
NM_001143991.2:c.350_352del NP_001137463.1:p.Glu117del
NM_001143992.2:c.350_352del MANE Select NP_001137464.1:p.Glu117del
NM_001143990.2:c.350_352del NP_001137462.1:p.Glu117del