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 ENSBTAG00000013952

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Description

heteroous nuclear ribonucleoprotein D [Source:VGNC Symbol;Acc:VGNC:52786]

Location

Primary_assembly 6: 97,143,335-97,160,733 reverse strand.

ARS-UCD2.0:CM008173.2

About this gene

This gene has 4 transcripts (splice variants), 197 orthologues and 47 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000075547.2	HNRNPD-204	1557	403aa	ENSBTAP00000066760.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M8I4	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 ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSBTAT00000018540.6	HNRNPD-203	1717	355aa	ENSBTAP00000018540.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6H6Y0	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,
ENSBTAT00000056365.2	HNRNPD-201	1498	306aa	ENSBTAP00000049251.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A5D9H5	APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSBTAT00000108982.1	HNRNPD-202	1356	336aa	ENSBTAP00000078543.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S5J8	APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2,

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Summary

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