Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34791108C>T , CM000677.2:g.34791108C>T | GRCh38 |
| NC_000015.9:g.35083309C>T , CM000677.1:g.35083309C>T | GRCh37 |
| NC_000015.8:g.32870601C>T | NCBI36 |
| NG_007553.1:g.9619G>A , LRG_388:g.9619G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_005159.5:c.990+6G>A (ACTC1) MANE Select | NP_005150.1:n.990+6G>A |
| ENST00000290378.6:c.990+6G>A (ACTC1) MANE Select | ENSP00000290378.4:n.990+6G>A |
| NM_005159.4:c.990+6G>A , LRG_388t1:c.990+6G>A (ACTC1) | NP_005150.1:n.990+6G>A |
| NR_120329.1:n.299+13677C>T (GJD2-DT) | |
| ENST00000290378.4:c.990+6G>A (ACTC1) | ENSP00000290378.4:n.990+6G>A |
| ENST00000560563.2:n.1890+6G>A (ACTC1) | |
| ENST00000647798.1:n.1084+6G>A (ACTC1) | |
| ENST00000650163.1:n.1070+6G>A (ACTC1) |