Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34791434A= , CM000677.2:g.34791434A= | GRCh38 |
| NC_000015.9:g.35083635A= , CM000677.1:g.35083635A= | GRCh37 |
| NC_000015.8:g.32870927A= | NCBI36 |
| NG_007553.1:g.9293T= , LRG_388:g.9293T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560563.2:n.1570T= (ACTC1) | ||
| ENST00000290378.6:c.809-139T= (ACTC1) MANE Select | ENSP00000290378.4:n.809-139T= | |
| ENST00000647798.1:n.903-139T= (ACTC1) | ||
| ENST00000650163.1:n.889-139T= (ACTC1) | ||
| ENST00000290378.4:c.809-139T= (ACTC1) | ENSP00000290378.4:n.809-139T= | |
| ENST00000557860.1:n.499-139T= (ACTC1) | ||
| NM_005159.4:c.809-139T= , LRG_388t1:c.809-139T= (ACTC1) | NP_005150.1:n.809-139T= | |
| NR_120329.1:n.299+14003A= (GJD2-DT) | ||
| NM_005159.5:c.809-139T= (ACTC1) MANE Select | NP_005150.1:n.809-139T= |