{{Rsnum
|rsid=104886308
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL4A5
|position=108696350
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COL4A5
}}{{omim
|id=303630
|rsnum=104886308
|variant=0015
}}{{ClinVar
|rsid=104886308
|Reversed=0
|FwdREF=G
|FwdALT=A,C,T
|REF=G
|ALT=A,C,T
|RSPOS=107939580
|CHROM=X
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110104
|GENEINFO=COL4A5:1287
|GENE_NAME=COL4A5
|GENE_ID=1287
|WGT=0
|VC=SNV
|CLNALLE=1; 2; 3
|CLNHGVS=NC_000023.10:g.107939580G>A; NC_000023.10:g.107939580G>C; NC_000023.10:g.107939580G>T
|CLNORIGIN=1
|CLNSRCID=
NBK1207; 303630.0015
|CLNSIG=5
|CLNCUI=
|CLNACC=
RCV000011213.2; RCV000021668.1; RCV000032091.1
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM;NOV
|CLNDBN=Alport syndrome, X-linked recessive
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1207:C1567742:301050:63:88917
|CLNSRC=GeneReviews; OMIM Allelic Variant
|Disease=Alport syndrome
}}{{PMID Auto
|PMID=9150741
|Title=Common ancestry of three Ashkenazi-American families with Alport syndrome and COL4A5 R1677Q.
}}

{{PMID Auto
|PMID=11223851
|Title=Efficient detection of Alport syndrome COL4A5 mutations with multiplex genomic PCR-SSCP.
}}{{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.
}}