{{Rsnum
|rsid=61126080
|Chromosome=12
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=KRT5
|position=52515066
|Gene_s=KRT5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=61126080
|Reversed=1
|FwdREF=G
|FwdALT=
|REF=GC
|ALT=G
|RSPOS=52908849
|CHROM=12
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168000000000002110200
|GENEINFO=KRT5:3852
|GENE_NAME=KRT5
|GENE_ID=3852
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.52908850delC
|CLNSRC=Epithelial Biology; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=KRT5:c.1649delG; NBK1369; 148040.0017
|CLNSIG=5
|CLNCUI=C1836284; C1836284; C1836284; C1836284
|CLNDBN=Epidermolysis bullosa simplex with migratory circinate erythema; not provided
|Disease=Epidermolysis bullosa simplex with migratory circinate erythema; not provided
|CLNACC=RCV000015761.25; RCV000056578.1
|Tags=RV;PM;PMC;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1369:C1836284:609352:158681
}}{{PMID Auto
|PMID=12925204
|Title=A usual frameshift and delayed termination codon mutation in keratin 5 causes a novel type of epidermolysis bullosa simplex with migratory circinate erythema.
}}

{{PMID Auto
|PMID=15324323
|Title=Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case.
}}