HRAS
This page contains an overview of the genetic variation in the HRAS gene, including its role in inherited cardiac disease. For more details, click on the links below, or for a specific variant, enter the HGVS variant here:
HRAS gene and transcript details
Gene Name
v-Ha-ras Harvey rat sarcoma viral oncogene homolog
Gene Links
Ensembl: ENSG00000174775 -
Locus Reference Genomic: LRG_506
Genomic Location
Chromosome 11 : 532,636 - 534,322 (reverse strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (567 bases) | Protein (189 aa) |
|---|---|---|
 |
ENST00000311189 | ENSP00000309845 |
 |
LRG_506t1 | LRG_506p1 |
 |
NM_005343.2 | |
 |
P01112 |
Summary of HRAS in Cardiomyopathies
HRAS variants in ExAC
Details of the protein-altering HRAS variants (missense, loss of function truncating, inframe indels and splice site regions) found in the ExAC database are shown below. To view lists of specific variants with links to detailed population frequency data, click on the variant numbers - for all or a particular variant class.
| Total Variants | Combined frequency of rare variants | |
|---|---|---|
| All Variants | 57 | 0.00074 |
| Truncating | 6 | 0.00009 |
| Missense | 40 | 0.00052 |
| Inframe | 0 | 0.00000 |
| Splice Site | 11 | 0.00013 |