{{Rsnum
|rsid=397515495
|Chromosome=X
|Orientation=plus
|geno1=(AACCTGGACCAATGGGACCAATGGGAACAC;AACCTGGACCAATGGGACCAATGGGAACAC)
|geno2=(AACCTGGACCAATGGGACCAATGGGAACAC;CCTCCTGG)
|geno3=(CCTCCTGG;CCTCCTGG)
|Gene=COL4A5
|position=108614949
|Gene_s=COL4A5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=AAACCTGGACCAATGGGACCAATGGGAACAC
|CHROM=X
|CLNACC=RCV000032065.1
|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.107858179_107858186delCCTCCTGGinsAACCTGGACCAATGGGACCAATGGGAACAC
|CLNSIG=5
|Disease=Alport syndrome
|FwdALT=AACCTGGACCAATGGGACCAATGGGAACAC
|FwdREF=CCTCCTGG
|GENEINFO=COL4A5:1287
|GENE_ID=1287
|GENE_NAME=COL4A5
|REF=ACCTCCTGG
|RSPOS=107858178
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=136
|rsid=397515495
}}