{{Rsnum
|rsid=281874751
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;T)
|geno3=(T;T)
|Gene=COL4A5
|position=108695405
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=CT
|CHROM=X
|CLNACC=RCV000032090.1
|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.107938635dupT
|CLNSIG=5
|Disease=Alport syndrome
|FwdALT=T
|REF=C
|RSPOS=107938631
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050268000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=281874751
|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.
}}