Canonical Allele Identifier: CA2697733685
Gene: RNASEL HGNC NCBI

Linked Data

dbSNP Id: rs2102371747
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.182586335_182586336insGATGAGATGGGGGCAGA , CM000663.2:g.182586335_182586336insGATGAGATGGGGGCAGA GRCh38
NC_000001.10:g.182555470_182555471insGATGAGATGGGGGCAGA , CM000663.1:g.182555470_182555471insGATGAGATGGGGGCAGA GRCh37
NC_000001.9:g.180822093_180822094insGATGAGATGGGGGCAGA NCBI36
NG_009024.2:g.5638_5639insTCTGCCCCCATCTCATC

Transcript Alleles

HGVS Amino-acid Change
ENST00000367559.7:c.471_472insTCTGCCCCCATCTCATC MANE Select ENSP00000356530.3:p.Lys158SerfsTer13
ENST00000539397.1:c.471_472insTCTGCCCCCATCTCATC ENSP00000440844.1:p.Lys158SerfsTer13
NM_021133.3:c.471_472insTCTGCCCCCATCTCATC NP_066956.1:p.Lys158SerfsTer13
XM_005245411.2:c.471_472insTCTGCCCCCATCTCATC XP_005245468.1:p.Lys158SerfsTer13
XR_001737359.1:n.754_755insTCTGCCCCCATCTCATC
XR_001737360.1:n.754_755insTCTGCCCCCATCTCATC
NM_021133.4:c.471_472insTCTGCCCCCATCTCATC MANE Select NP_066956.1:p.Lys158SerfsTer13
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