{{Rsnum
|rsid=387907180
|Chromosome=13
|Orientation=plus
|geno1=(-;-)
|geno2=(-;CTGTAGTGAAGAATCAAAAT)
|geno3=(CTGTAGTGAAGAATCAAAAT;CTGTAGTGAAGAATCAAAAT)
|Gene=ALG11
|position=52024353
|Gene_s=ALG11,UTP14C
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=13
|CLNACC=RCV000024339.1
|CLNALLE=1
|CLNDBN=Congenital disorder of glycosylation type 1P
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1332:C3150913:613661:280071
|CLNHGVS=NC_000013.10:g.52598489_52598508del20
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613666.0002
|Disease=Congenital disorder of glycosylation type 1P
|FwdREF=CTGTAGTGAAGAATCAAAAT
|REF=TCTGTAGTGAAGAATCAAAAT
|RSPOS=52598488
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387907180
|GENEINFO=ALG11:440138; UTP14C:9724
|GENE_ID=440138; 9724
|GENE_NAME=ALG11; UTP14C
}}