MYH11
This page contains an overview of the genetic variation in the MYH11 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:
MYH11 gene and transcript details
Gene Name
myosin, heavy chain 11, smooth muscle
Gene Links
Ensembl: ENSG00000133392 -
Locus Reference Genomic:
Genomic Location
Chromosome 16 : 15,797,848 - 15,932,109 (reverse strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (5916 bases) | Protein (1972 aa) |
|---|---|---|
 |
ENST00000300036 | ENSP00000300036 |
 |
||
 |
NM_002474.2 | |
 |
P35749 |
Summary of MYH11 in Cardiomyopathies
MYH11 variants in ExAC
Details of the protein-altering MYH11 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 | 782 | 0.01204 |
| Truncating | 16 | 0.00013 |
| Missense | 638 | 0.00981 |
| Inframe | 7 | 0.00024 |
| Splice Site | 121 | 0.00187 |