{{Rsnum
|rsid=104886427
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CT)
|geno3=(CT;CT)
|Gene=COL4A5
|position=108440174
|Gene_s=COL4A5,COL4A6
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=104886427
|Reversed=0
|FwdREF=CT
|FwdALT=
|REF=CCT
|ALT=C
|RSPOS=107683403
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050068000000000002110200
|GENEINFO=COL4A5:1287
|GENE_NAME=COL4A5
|GENE_ID=1287
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.107683404_107683405delCT
|CLNSRC=ARUP_COL4A5
|CLNSIG=5
|CLNCUI=C1567741
|CLNDBN=Alport syndrome, X-linked recessive
|Disease=Alport syndrome
|CLNACC=RCV000021106.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
}}{{PMID Auto
|PMID=19693995
|Title=Novel human pathological mutations. Gene symbol: COL4A5. Disease: Alport syndrome.
}}
{{omim
|id=301050
|rsnum=104886427
}}