Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34794278A= , CM000677.2:g.34794278A= | GRCh38 |
| NC_000015.9:g.35086479A= , CM000677.1:g.35086479A= | GRCh37 |
| NC_000015.8:g.32873771A= | NCBI36 |
| NG_007553.1:g.6449T= , LRG_388:g.6449T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560563.2:n.235+402T= (ACTC1) | ||
| ENST00000290378.6:c.129+402T= (ACTC1) MANE Select | ENSP00000290378.4:n.129+402T= | |
| ENST00000290378.4:c.129+402T= (ACTC1) | ENSP00000290378.4:n.129+402T= | |
| NM_005159.4:c.129+402T= , LRG_388t1:c.129+402T= (ACTC1) | NP_005150.1:n.129+402T= | |
| NR_120329.1:n.300-16218A= (GJD2-DT) | ||
| NM_005159.5:c.129+402T= (ACTC1) MANE Select | NP_005150.1:n.129+402T= |