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

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Gene: RRAS ENSG00000126458

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Description

related RAS viral (r-ras) oncogene homolog [Source:HGNC Symbol;Acc:10447]

Location

Chromosome 19: 50,138,549-50,143,458 reverse strand.

GRCh37:CM000681.1

About this gene

This gene has 2 transcripts (splice variants), 12 paralogues and is associated with 4 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000246792.3	RRAS-001	1044	218aa	ENSP00000246792.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS12774	P10301	NM_006270.3	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000601532.1	RRAS-002	634	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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