Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34793289G>A , CM000677.2:g.34793289G>A | GRCh38 |
| NC_000015.9:g.35085490G>A , CM000677.1:g.35085490G>A | GRCh37 |
| NC_000015.8:g.32872782G>A | NCBI36 |
| NG_007553.1:g.7438C>T , LRG_388:g.7438C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560563.2:n.516C>T (ACTC1) | ||
| ENST00000290378.6:c.410C>T (ACTC1) MANE Select | ENSP00000290378.4:p.Ala137Val | |
| ENST00000647798.1:n.548+9C>T (ACTC1) | ||
| ENST00000648556.1:n.567C>T (ACTC1) | ||
| ENST00000650163.1:n.490C>T (ACTC1) | ||
| ENST00000290378.4:c.410C>T (ACTC1) | ENSP00000290378.4:p.Ala137Val | |
| NM_005159.4:c.410C>T , LRG_388t1:c.410C>T (ACTC1) | NP_005150.1:p.Ala137Val | |
| NR_120329.1:n.299+15858G>A (GJD2-DT) | ||
| NM_005159.5:c.410C>T (ACTC1) MANE Select | NP_005150.1:p.Ala137Val |