Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
Ontologies
- GO: Anatomical entity
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: EIF2S1 ENSPTRG00000006462

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Description

eukaryotic translation initiation factor 2 subunit alpha [Source:VGNC Symbol;Acc:VGNC:3438]

Location

Chromosome 14: 51,732,633-51,758,616 forward strand.

Pan_tro_3.0:CM000328.3

About this gene

This gene has 1 transcript (splice variant) and 237 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000011836.3	EIF2S1-201	4235	315aa	ENSPTRP00000010961.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2W506 H2Q8H4	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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