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Protein Ontology report - cartilage oligomeric matrix protein sequence variant 32 (human) PR:000000256 - http://purl.obolibrary.org/obo/PR_000000256        Annotations       Ontology Information Show OBO stanza / PAF / GPI   PRO ID PR:000000256      PRO name cartilage oligomeric matrix protein sequence variant 32 (human)    Synonyms PRO-Short-label: EXACT: hCOMP/var:32 PRO-proteoform-std: EXACT: UniProtKB:P49747, 21-366, 369-757 NARROW: UniProtKB:P49747-1, 21-366, 369-757   Definition "A cartilage oligomeric matrix protein (human) that has a two-residue deletion at the positions equivalent to region 367-368 of the amino acid sequence represented by UniProtKB:P49747-1. Example: UniProtKB:P49747-1, 21-366, 369-757." [PRO:CNA, PRO:DAN]    PRO Category organism-sequence    Parent PR:P49747 cartilage oligomeric matrix protein (human)   Taxon NCBITaxon:9606 Homo sapiens   Term Hierarchy   Visualization DAG: OLS: Back to top Related Cross References   Db identifiers UniProtKB_VAR:VAR_007621 Back to top Functional Annotation (PRO-centric view) Switch to GO Centric View    PRO Term GO Annotation Evidence PR:000000256 hCOMP/var:32 Example: UniProtKB:P49747-1, 21-366, 369-757 associated_with_disease_progression DO:12721 multiple epiphyseal dysplasia UniProtKB_VAR:VAR_007621