{{Rsnum
|rsid=80338804
|Chromosome=15
|Orientation=plus
|geno1=(-;-)
|geno2=(-;AG)
|geno3=(AG;AG)
|Gene=CAPN3
|position=42410982
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=CAPN3
}}{{omim
|id=114240
|rsnum=80338804
|variant=0006
}}{{ClinVar
|rsid=80338804
|Reversed=0
|FwdREF=AG
|FwdALT=
|REF=TAG
|ALT=TTCATCT
|RSPOS=42703179
|CHROM=15
|dbSNPBuildID=138
|SSR=0
|SAO=1
|VP=0x050368000000000002110200
|GENEINFO=CAPN3:825
|GENE_NAME=CAPN3
|GENE_ID=825
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.42703180_42703181delAGinsTCATCT
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1313; 114240.0006
|CLNSIG=5
|CLNCUI=C1869123; C1869123
|CLNDBN=Limb-girdle muscular dystrophy, type 2A; Myositis, eosinophilic
|Disease=Limb-girdle muscular dystrophy; Myositis
|CLNACC=RCV000019184.26; RCV000019185.26
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=NBK1313:NBK1408:C1869123:253600:267; C1299884
|FwdALT=TCATCT
}}{{PMID|9150160|OA=1
}} Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.

{{PMID|9762961}} Limb-girdle muscular dystrophy in Guipuzcoa (Basque Country, Spain).

{{PMID|9777948|OA=1
}} Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A.

{{PMID|12461690}} Clinical variability in calpainopathy: what makes the difference?

{{PMID|16607617}} CAPN3 mutations in patients with idiopathic eosinophilic myositis.