{{Rsnum
|rsid=104886359
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;TCCTGGACTTGATGTTCCAGGACC)
|geno3=(TCCTGGACTTGATGTTCCAGGACC;TCCTGGACTTGATGTTCCAGGACC)
|Gene=COL4A5
|position=108620299
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNACC=RCV000021414.1
|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.107863529_107863552del24
|CLNSIG=5
|Disease=Alport syndrome
|FwdREF=TCCTGGACTTGATGTTCCAGGACC
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=CTCCTGGACTTGATGTTCCAGGACC
|RSPOS=107863528
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=132
|rsid=104886359
}}{{PMID Auto
|PMID=15780079
|Title=Detection of mutations in the COL4A5 gene by analyzing cDNA of skin fibroblasts.
}}