{{Rsnum
|rsid=386833969
|Chromosome=13
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AT)
|geno3=(AT;AT)
|Gene=CLN5
|position=77000920
|Gene_s=CLN5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=13
|CLNACC=RCV000002673.3
|CLNALLE=1
|CLNDBN=Ceroid lipofuscinosis neuronal 5
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1428:C1850442:256731:168491:228360
|CLNHGVS=NC_000013.10:g.77575055_77575056delAT
|CLNSIG=5
|Disease=Ceroid lipofuscinosis neuronal 5
|FwdREF=AT
|REF=CAT
|RSPOS=77575052
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833969
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1428; 608102.0001
|GENEINFO=CLN5:1203
|GENE_ID=1203
|GENE_NAME=CLN5
}}{{PMID Auto
|PMID=9662406
|Title=CLN5, a novel gene encoding a putative transmembrane protein mutated in Finnish variant late infantile neuronal ceroid lipofuscinosis.
}}

{{PMID Auto
|PMID=21990111
|Title=Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses.
}}