Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: HNRNPD ENSSSCG00000009249

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Description

heteroous nuclear ribonucleoprotein D [Source:VGNC Symbol;Acc:VGNC:88919]

Location

Primary_assembly 8: 135,844,487-135,862,626 forward strand.

Sscrofa11.1:CM000819.5

About this gene

This gene has 4 transcripts (splice variants), 197 orthologues and 39 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000010129.5	HNRNPD-203	1750	355aa	ENSSSCP00000009863.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1TAE1 F1RVC9	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,
ENSSSCT00000046827.2	HNRNPD-202	1668	336aa	ENSSSCP00000040803.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287AAI4 A0A4X1TBX5	APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT1,
ENSSSCT00000044295.2	HNRNPD-204	1575	287aa	ENSSSCP00000031411.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZIN0 A0A4X1TCD8	-
ENSSSCT00000061534.2	HNRNPD-201	1530	306aa	ENSSSCP00000038114.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A480M1B4 A0A4X1TB95	-

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Summary

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