{{Rsnum
|rsid=104886277
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL4A5
|position=108687509
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=104886277
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=107930739
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050068000000000002110100
|GENEINFO=COL4A5:1287
|GENE_NAME=COL4A5
|GENE_ID=1287
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.107930739G>A; NC_000023.10:g.107930739G>C
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000021612.1; RCV000021611.1
|Tags=PM;PMC;OTHERKG;LSD;OM
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
|Disease=Alport syndrome
}}{{PMID Auto
|PMID=10094548
|Title=Detection of mutations in COL4A5 in patients with Alport syndrome.
}}

{{PMID Auto
|PMID=19281745
|Title=Atypical Alport syndrome associated with a novel COL4A5 mutation.
}}
{{omim
|id=301050
|rsnum=104886277
}}