Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Hras ENSRNOG00000016611

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Description

HRas proto-oncogene, GTPase [Source:RGD Symbol;Acc:2827]

Gene Synonyms

H-Ras-1, HRAS1, c-H-ras, p21ras

Location

Primary_assembly 1: 205,725,975-205,729,590 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 293 orthologues, 38 paralogues and is associated with 115 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000079464.3	Hras-202	1559	290aa	ENSRNOP00000069770.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R1F7	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,
ENSRNOT00000126494.1	Hras-203	1042	271aa	ENSRNOP00000106430.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000022363.8	Hras-201	852	190aa	ENSRNOP00000022363.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QCK8	-

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Summary

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