Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34792234C>G , CM000677.2:g.34792234C>G | GRCh38 |
| NC_000015.9:g.35084435C>G , CM000677.1:g.35084435C>G | GRCh37 |
| NC_000015.8:g.32871727C>G | NCBI36 |
| NG_007553.1:g.8493G>C , LRG_388:g.8493G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000560563.2:n.770G>C (ACTC1) | ||
| ENST00000290378.6:c.664G>C (ACTC1) MANE Select | ENSP00000290378.4:p.Ala222Pro | |
| ENST00000647798.1:n.758G>C (ACTC1) | ||
| ENST00000650163.1:n.744G>C (ACTC1) | ||
| ENST00000290378.4:c.664G>C (ACTC1) | ENSP00000290378.4:p.Ala222Pro | |
| ENST00000557860.1:n.354G>C (ACTC1) | ||
| ENST00000560563.1:n.163G>C (ACTC1) | ||
| NM_005159.4:c.664G>C , LRG_388t1:c.664G>C (ACTC1) | NP_005150.1:p.Ala222Pro | |
| NR_120329.1:n.299+14803C>G (GJD2-DT) | ||
| NM_005159.5:c.664G>C (ACTC1) MANE Select | NP_005150.1:p.Ala222Pro |