{% for transcript in gene.transcripts %}
{% if transcript.refseq_identifiers %}
{% set n_primary_txs.count = n_primary_txs.count + 1 %}
{% endif %}
{% if transcript.refseq_identifiers and n_primary_txs.count <= 5 or transcript.is_canonical or transcript.is_disease_associated or transcript.is_primary %}
{{transcript.transcript_id}}, RefSeq:[{{ transcript.refseq_identifiers|join(", ") or "-" }}], {{ (transcript.coding_sequence_name or '')|truncate(20, True) }}, {{ (transcript.protein_sequence_name or '')|truncate(20, True) }}
{% if transcript.is_canonical %}
C
{% endif %}
{% if transcript.is_disease_associated %}
D
{% endif %}
{% if transcript.is_primary %}
hgnc primary:{{transcript.refseq_id}}
{% endif %}
{% endif %}
{% endfor %}
{% if n_primary_txs.count > 5 %}
.. other transcripts available for this variant are not shown.