Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34793000C>A , CM000677.2:g.34793000C>A | GRCh38 |
| NC_000015.9:g.35085201C>A , CM000677.1:g.35085201C>A | GRCh37 |
| NC_000015.8:g.32872493C>A | NCBI36 |
| NG_007553.1:g.7727G>T , LRG_388:g.7727G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005159.5:c.454+245G>T (ACTC1) MANE Select | NP_005150.1:n.454+245G>T |
| ENST00000290378.6:c.454+245G>T (ACTC1) MANE Select | ENSP00000290378.4:n.454+245G>T |
| NM_005159.4:c.454+245G>T , LRG_388t1:c.454+245G>T (ACTC1) | NP_005150.1:n.454+245G>T |
| NR_120329.1:n.299+15569C>A (GJD2-DT) | |
| ENST00000290378.4:c.454+245G>T (ACTC1) | ENSP00000290378.4:n.454+245G>T |
| ENST00000560563.2:n.560+245G>T (ACTC1) | |
| ENST00000647798.1:n.548+298G>T (ACTC1) | |
| ENST00000648556.1:n.611+245G>T (ACTC1) | |
| ENST00000650163.1:n.534+245G>T (ACTC1) |