Canonical Allele Identifier: CA304607181
Gene: RPL36 HGNC NCBI

Linked Data

dbSNP Id: rs116840814

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5691556_5691557del , CM000681.2:g.5691556_5691557del GRCh38
NC_000019.9:g.5691567_5691568del , CM000681.1:g.5691567_5691568del GRCh37
NC_000019.8:g.5642567_5642568del NCBI36
NG_017015.1:g.6296_6297del
NG_033142.1:g.33898_33899del

Transcript Alleles

HGVS Amino-acid change
ENST00000347512.8:c.253_254del MANE Select ENSP00000252543.3:p.Arg85GlufsTer?
ENST00000347512.7:c.253_254del ENSP00000252543.3:p.Arg85GlufsTer?
ENST00000394580.2:c.253_254del ENSP00000378081.2:p.Arg85GlufsTer?
ENST00000577222.5:c.253_254del ENSP00000464342.1:p.Arg85GlufsTer?
ENST00000579446.1:c.*46_*47del ENSP00000464613.1:n.*46_*47del
ENST00000579649.5:c.253_254del ENSP00000462609.1:p.Arg85GlufsTer?
NM_015414.3:c.253_254del NP_056229.2:p.Arg85GlufsTer?
NM_033643.2:c.253_254del NP_378669.1:p.Arg85GlufsTer?
NM_033643.3:c.253_254del MANE Select NP_378669.1:p.Arg85GlufsTer?
NM_015414.4:c.253_254del NP_056229.2:p.Arg85GlufsTer?