{{Rsnum
|rsid=104886373
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AG)
|geno3=(AG;AG)
|Gene=COL4A5
|position=108624246
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=X
|CLNALLE=1
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=OMIM
|CLNDSDBID=301050
|CLNHGVS=NC_000023.10:g.107867476_107867477delAG
|CLNSIG=4
|Disease=Alport syndrome
|FwdREF=AG
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=GAG
|RSPOS=107867475
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;NSF;REF;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068001201000002110200
|WGT=1
|dbSNPBuildID=132
|rsid=104886373
}}{{PMID Auto
|PMID=10094548
|Title=Detection of mutations in COL4A5 in patients with Alport syndrome.
}}