Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: HNRNPF ENSPTRG00000002446

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Description

heteroous nuclear ribonucleoprotein F [Source:VGNC Symbol;Acc:VGNC:4712]

Location

Chromosome 10: 45,203,061-45,204,308 reverse strand.

Pan_tro_3.0:CM000324.3

About this gene

This gene has 1 transcript (splice variant), 113 orthologues and 11 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000004547.6	HNRNPF-201	1248	415aa	ENSPTRP00000050686.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2X7P4 G2HIV6	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 P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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