Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34794799C>A , CM000677.2:g.34794799C>A | GRCh38 |
| NC_000015.9:g.35087000C>A , CM000677.1:g.35087000C>A | GRCh37 |
| NC_000015.8:g.32874292C>A | NCBI36 |
| NG_007553.1:g.5928G>T , LRG_388:g.5928G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560563.2:n.116G>T (ACTC1) | ||
| ENST00000290378.6:c.10G>T (ACTC1) MANE Select | ENSP00000290378.4:p.Asp4Tyr | |
| ENST00000290378.4:c.10G>T (ACTC1) | ENSP00000290378.4:p.Asp4Tyr | |
| NM_005159.4:c.10G>T , LRG_388t1:c.10G>T (ACTC1) | NP_005150.1:p.Asp4Tyr | |
| NR_120329.1:n.300-15697C>A (GJD2-DT) | ||
| NM_005159.5:c.10G>T (ACTC1) MANE Select | NP_005150.1:p.Asp4Tyr |