Submission field descriptions

The following table contains detailed information regarding the different data fields required for submission to the IPD-IMGT/HLA Database, including descriptions.

Submission Metadata

Information regarding the submission itself, including submitter ID, email and local name of the sequence.

FieldDescription
Submitter IDYour IPD-IMGT/HLA Submitter ID
EmailEmail associated with submission
Local NameLocal designation of the sequence in your lab. Should not resemble official nomenclature
INSDC DatabaseAll submissions to the database must be included in an public sequence database such as GenBank/ENA/DDBJ. IPD-IMGT/HLA can now broker submissions to ENA on your behalf
INSDC AccessionIf already submitted to INSDC, a sequence accession number can be included in submission to IPD-IMGT/HLA
ENA Study AccessionIf you wish IPD-IMGT/HLA to broker sequences to ENA on your behalf a registered ENA study accession can be provided

Sequence Information

Information regarding the sequence being submitted, including locus, closest named allele, nucleotide sequence and feature annotation.

FieldDescription
LocusThe HLA or HLA related locus to be submitted (e.g. HLA-A, HLA-B, HLA-DRB1, MICA)
Sequence TypeThe level of the sequence (coding/genomic) used to annotate feature coordinates
Closest Named AlleleAn existing allele in the IPD-IMGT/HLA Database for use in describing the submitted sequence. If a genomic sequence is being submitted a full length closest allele must be provided. For more information on closest named alleles please see our Submission FAQs.
DescriptionA human readable description of the submitted sequence compared to the Closest Named Allele, including all polymorphisms in all regions covered by the submission. The Closest Named Allele must be included in the sequence description. We do not require descriptions in a particular format, however suggest reading HGVS Recommendations for the Description of Sequence Variants for guidance.
Nucleotide SequenceThe nucleotide sequence to be submitted as plain text. Please read our submission guidelines for more information.
Sequence FeaturesAutomatic exon/intron feature annotation through our web tool is provided by the Sequence Feature Annotation Tool. For API submitters please refer to the SFAT API documentation for more information.

Cell Information

Information regarding the cell source of the sequence, including ancestry, cell owner and HLA typing, as well as methodology used to generate the sequence.

Any sequence identified in a patient with a malignant disease must be confirmed in the germ line before submitting to the IPD-IMGT/HLA Database.

FieldDescription
Cell NameA unique identifier for the cell source of the submitted sequence. This must not contain any personally identifiable information.
AliasAny other names the cell has been known by. This is particularly useful of the sequence comes from an established cell line.
AncestryInformation on the ancestry of the cell source, our ancestry identifiers are taken from the Human Ancestry Ontology.
Broad AncestryBroad ancestral group (e.g. African, Asian, European)
Local DesignationSpecific population an individual belongs to, or multiple populations for an admixed individual
CountryThe country of origin of the individual
RegionThe global region of origin of the individual, if the country is not known
SexThe biological sex of the individual
ConsanguineousWhether the individual is consanguineous
HomozygousWhether the individual is homozygous for the HLA region
Cell OwnerInformation on the original laboratory that isolated the cell
Lab of originThe name of the laboratory where the cell was originally isolated
Lab ContactA named individual to contact regarding the cell
Material AvaiableIf and what material of this cell is available for resequencing
Cell BankIf and what cell bank can this cell be obtained from
IHIW CellIs this cell from the collection developedd by the International Histocompatibility and Immunogenetics Workshops
HLA TypingThe HLA typing for the cell source. Minimum HLA typing requirements include both alleles for HLA-A, -B, -DRB1, and the submitted locus

Methodology Information

Information regarding the methodology used to generate the sequence, including sequencing method, target enrichment and any secondary methods used to confirm polymorphisms.

FieldDescription
Sequencing MethodSequencing method or platform used to generate the nucleotide sequence
Target EnrichmentMethod used to amplify the gene for sequencing
Secondary MethodsA polymorphism may also be confirmed using a secondary method such as PCR-SSO, PCR-SSP