{{Rsnum
|rsid=386833975
|Chromosome=13
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=CLN5
|position=76995990
|Gene_s=CLN5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=13
|CLNACC=RCV000049952.1
|CLNALLE=1
|CLNDBN=Ceroid lipofuscinosis neuronal 5
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1428:C1850442:256731:168491:228360
|CLNHGVS=NC_000013.10:g.77570125A>G
|CLNSIG=4
|Disease=Ceroid lipofuscinosis neuronal 5
|FwdALT=G
|FwdREF=A
|REF=A
|RSPOS=77570125
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833975
|GENEINFO=CLN5:1203
|GENE_ID=1203
|GENE_NAME=CLN5
}}{{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.
}}