{{Rsnum
|rsid=281874732
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=COL4A5
|position=108686067
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=X
|CLNACC=RCV000032082.1
|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.107929297delG
|CLNSIG=5
|Disease=Alport syndrome
|FwdREF=G
|REF=TG
|RSPOS=107929295
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=281874732
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
}}{{PMID Auto
|PMID=21505094
|Title=Twenty-one novel mutations identified in the COL4A5 gene in Chinese patients with X-linked Alport's syndrome confirmed by skin biopsy.
}}