{{Rsnum
|rsid=104886404
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;TCCT)
|geno3=(TCCT;TCCT)
|Gene=COL4A5
|position=108681833
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=104886404
|Reversed=0
|FwdALT=TCCT
|REF=T
|ALT=TTCCT
|RSPOS=107925063
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=0
|VP=0x050068001201000002110200
|GENEINFO=COL4A5:1287
|GENE_NAME=COL4A5
|GENE_ID=1287
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000023.10:g.107925063_107925064insTCCT
|CLNSRC=ARUP_COL4A5
|CLNSIG=4
|CLNCUI=C1567741
|CLNDBN=Alport syndrome, X-linked recessive
|Disease=Alport syndrome
|CLNACC=SCV000042253.1
|Tags=PM;PMC;NSF;REF;OTHERKG;LSD;OM
|CLNDSDB=OMIM
|CLNDSDBID=301050
}}{{PMID Auto
|PMID=8651296
|Title=X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.
|OA=1
}}
{{omim
|id=301050
|rsnum=104886404
}}