{{Rsnum
|rsid=104886330
|Chromosome=X
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AACCTGGTTTGCCAGGTCTCCCAGGTCCTCCAGGTAA)
|geno3=(AACCTGGTTTGCCAGGTCTCCCAGGTCCTCCAGGTAA;AACCTGGTTTGCCAGGTCTCCCAGGTCCTCCAGGTAA)
|Gene=COL4A5
|position=108595569
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=X
|CLNALLE=1
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=OMIM
|CLNDSDBID=301050
|CLNHGVS=NC_000023.10:g.107838799_107838835del37
|CLNSIG=4
|Disease=Alport syndrome
|FwdREF=AACCTGGTTTGCCAGGTCTCCCAGGTCCTCCAGGTAA
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=CAACCTGGTTTGCCAGGTCTCCCAGGTCCTCCAGGTAA
|RSPOS=107838798
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;INT;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068080001000002110200
|WGT=1
|dbSNPBuildID=132
|rsid=104886330
}}{{PMID Auto
|PMID=8651296
|Title=X-linked Alport syndrome: an SSCP-based mutation survey over all 51 exons of the COL4A5 gene.
|OA=1
}}