{{Rsnum
|rsid=80356816
|Chromosome=12
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=KRT5
|position=52515066
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Status=Merged
|Merged=61126080
|Gene_s=KRT5
}}{{omim
|id=148040
|rsnum=80356816
|variant=0017
}}{{ClinVar
|rsid=80356816
|Reversed=1
|FwdREF=G
|FwdALT=
|REF=GC
|ALT=G
|RSPOS=52908849
|CHROM=12
|dbSNPBuildID=131
|SSR=0
|SAO=0
|VP=050168001205000002110200
|GENEINFO=KRT5:3852
|GENE_NAME=KRT5
|GENE_ID=3852
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000012.11:g.52908850delC
|CLNSRC=OMIM Allelic Variant; GeneReviews
|CLNORIGIN=0
|CLNSRCID=148040.0017; 148040.0017; NBK1369; NBK1369
|CLNSIG=5
|CLNCUI=C1836284; C1836284; C1836284; C1836284
|CLNDBN=Epidermolysis Bullosa Simplex
|Disease=Epidermolysis Bullosa Simplex
|CLNACC=SCV000036026.1; SCV000036026.1; SCV000040663.1; SCV000040663.1
|Tags=RV;PM;PMC;SLO;NSF;REF;ASP;OTHERKG;LSD;OM
}}{{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.
}}