Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34793473C>G , CM000677.2:g.34793473C>G | GRCh38 |
| NC_000015.9:g.35085674C>G , CM000677.1:g.35085674C>G | GRCh37 |
| NC_000015.8:g.32872966C>G | NCBI36 |
| NG_007553.1:g.7254G>C , LRG_388:g.7254G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000560563.2:n.332G>C (ACTC1) | ||
| ENST00000290378.6:c.226G>C (ACTC1) MANE Select | ENSP00000290378.4:p.Gly76Arg | |
| ENST00000647798.1:n.373G>C (ACTC1) | ||
| ENST00000648556.1:n.383G>C (ACTC1) | ||
| ENST00000650163.1:n.306G>C (ACTC1) | ||
| ENST00000290378.4:c.226G>C (ACTC1) | ENSP00000290378.4:p.Gly76Arg | |
| NM_005159.4:c.226G>C , LRG_388t1:c.226G>C (ACTC1) | NP_005150.1:p.Gly76Arg | |
| NR_120329.1:n.299+16042C>G (GJD2-DT) | ||
| NM_005159.5:c.226G>C (ACTC1) MANE Select | NP_005150.1:p.Gly76Arg |