{{Rsnum
|rsid=201220208
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=COL4A5
|position=108692786
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=X
|CLNACC=RCV000021628.1
|CLNALLE=1
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
|CLNHGVS=NC_000023.10:g.107936016C>A
|CLNSIG=5
|Disease=Alport syndrome
|FwdALT=A
|FwdREF=C
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=C
|RSPOS=107936016
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050268000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=201220208
}}{{PMID Auto
|PMID=8651296
|Title=X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.
|OA=1
}}