{{Rsnum
|rsid=104886445
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;GGGACTT)
|geno3=(GGGACTT;GGGACTT)
|Gene=COL4A5
|position=108580532
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNALLE=1
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=OMIM
|CLNDSDBID=301050
|CLNHGVS=NC_000023.10:g.107823762_107823768delGGGACTT
|CLNSIG=4
|Disease=Alport syndrome
|FwdREF=GGGACTT
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=AGGGACTT
|RSPOS=107823761
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;ASS;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068200001000002110200
|WGT=1
|dbSNPBuildID=132
|rsid=104886445
}}{{PMID Auto
|PMID=8648925
|Title=The COL4A5 gene in Japanese Alport syndrome patients: spectrum of mutations of all exons. The Japanese Alport Network.
}}