{{Rsnum
|rsid=104886354
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AGTCCAGGGATCCCCGGAGCACCTGGTCCTATAGGA)
|geno3=(AGTCCAGGGATCCCCGGAGCACCTGGTCCTATAGGA;AGTCCAGGGATCCCCGGAGCACCTGGTCCTATAGGA)
|Gene=COL4A5
|position=108620339
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNALLE=1
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=OMIM
|CLNDSDBID=301050
|CLNHGVS=NC_000023.10:g.107863569_107863604del36
|CLNSIG=4
|Disease=Alport syndrome
|FwdREF=AGTCCAGGGATCCCCGGAGCACCTGGTCCTATAGGA
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=CAGTCCAGGGATCCCCGGAGCACCTGGTCCTATAGGA
|RSPOS=107863568
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000001000002110200
|WGT=1
|dbSNPBuildID=132
|rsid=104886354
}}{{PMID Auto
|PMID=10862091
|Title=Spectrum of COL4A5 mutations in Finnish Alport syndrome patients.
}}