{{Rsnum
|rsid=80356800
|Chromosome=11
|Orientation=minus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=CPT1A
|Gene_s=CPT1A
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|position=68793334
}}{{ClinVar
|ALT=T
|CHROM=11
|CLNALLE=1
|CLNDBN=Carnitine palmitoyltransferase I deficiency
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1527:C0342789:255120:156:238001003
|CLNHGVS=NC_000011.9:g.68560802delC
|CLNORIGIN=0
|CLNSIG=5
|Disease=Carnitine palmitoyltransferase I deficiency
|FwdREF=G
|GENEINFO=CPT1A:1374
|GENE_ID=1374
|GENE_NAME=CPT1A
|REF=TC
|RSPOS=68560801
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050368000000000002110200
|WGT=0
|dbSNPBuildID=131
|rsid=80356800
|CLNACC=RCV000009637.4
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK1527; 600528.0010
}}{{PMID Auto
|PMID=14517221
|Title=Functional and structural basis of carnitine palmitoyltransferase 1A deficiency.
}}