##gff-version 3
P24298	UniProtKB	Initiator methionine	1	1	.	.	.	Note=Removed;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:1931970;Dbxref=PMID:1931970	
P24298	UniProtKB	Chain	2	496	.	.	.	ID=PRO_0000123933;Note=Alanine aminotransferase 1	
P24298	UniProtKB	Modified residue	2	2	.	.	.	Note=N-acetylalanine;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:1931970;Dbxref=PMID:1931970	
P24298	UniProtKB	Modified residue	22	22	.	.	.	Note=Phosphothreonine;Ontology_term=ECO:0007744;evidence=ECO:0007744|PubMed:24275569;Dbxref=PMID:24275569	
P24298	UniProtKB	Modified residue	314	314	.	.	.	Note=N6-(pyridoxal phosphate)lysine;Ontology_term=ECO:0000250;evidence=ECO:0000250	
P24298	UniProtKB	Natural variant	14	14	.	.	.	ID=VAR_000561;Note=In allele GPT*2. H->N;Ontology_term=ECO:0000269,ECO:0000269;evidence=ECO:0000269|PubMed:9119391,ECO:0000269|Ref.4;Dbxref=dbSNP:rs1063739,PMID:9119391	
P24298	UniProtKB	Natural variant	430	430	.	.	.	ID=VAR_075711;Note=Found in patient with Joubert syndrome%3B uncertain significance. E->Q;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26477546;Dbxref=dbSNP:rs141505249,PMID:26477546	
P24298	UniProtKB	Natural variant	452	452	.	.	.	ID=VAR_075712;Note=Found in patient with Joubert syndrome%3B uncertain significance. V->L;Ontology_term=ECO:0000269;evidence=ECO:0000269|PubMed:26477546;Dbxref=dbSNP:rs147998249,PMID:26477546	
P24298	UniProtKB	Sequence conflict	4	7	.	.	.	Note=STGD->RRGN;Ontology_term=ECO:0000305;evidence=ECO:0000305	
P24298	UniProtKB	Sequence conflict	39	39	.	.	.	Note=G->S;Ontology_term=ECO:0000305;evidence=ECO:0000305	
P24298	UniProtKB	Sequence conflict	222	222	.	.	.	Note=H->A;Ontology_term=ECO:0000305;evidence=ECO:0000305