Canonical Allele Identifier: CA278866
Gene: TNFSF11 HGNC NCBI

Linked Data

ClinVar Variation Id: 6975
ClinVar RCV Id: RCV000007390
dbSNP Id: rs863223288

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.42606792_42606793del , CM000675.2:g.42606792_42606793del GRCh38
NC_000013.10:g.43180928_43180929del , CM000675.1:g.43180928_43180929del GRCh37
NC_000013.9:g.42078928_42078929del NCBI36
NG_008990.1:g.49057_49058del

Transcript Alleles

HGVS Amino-acid change
ENST00000398795.7:c.828_829del MANE Select ENSP00000381775.3:p.Val277TrpfsTer5
ENST00000239849.8:c.687_688del ENSP00000239849.7:p.Val230TrpfsTer5
ENST00000358545.6:c.609_610del ENSP00000351347.2:p.Val204TrpfsTer5
ENST00000398795.6:c.828_829del ENSP00000381775.3:p.Val277TrpfsTer5
ENST00000405262.6:c.609_610del ENSP00000384042.2:p.Val204TrpfsTer5
ENST00000544862.5:c.609_610del ENSP00000444913.1:p.Val204TrpfsTer5
NM_003701.3:c.828_829del NP_003692.1:p.Val277TrpfsTer5
NM_033012.3:c.609_610del NP_143026.1:p.Val204TrpfsTer5
XM_011535280.1:c.609_610del XP_011533582.1:p.Val204TrpfsTer5
XM_011535280.2:c.609_610del XP_011533582.1:p.Val204TrpfsTer5
XM_017020802.1:c.666_667del XP_016876291.1:p.Val223TrpfsTer5
XM_017020803.2:c.609_610del XP_016876292.1:p.Val204TrpfsTer5
NM_003701.4:c.828_829del MANE Select NP_003692.1:p.Val277TrpfsTer5
NM_033012.4:c.609_610del NP_143026.1:p.Val204TrpfsTer5