Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.73251912G= , CM000672.2:g.73251912G= | GRCh38 |
| NC_000010.10:g.75011670G= , CM000672.1:g.75011670G= | GRCh37 |
| NC_000010.9:g.74681676G= | NCBI36 |
| NG_008096.1:g.5782C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372945.8:c.125C= (MRPS16) MANE Select | ENSP00000362036.3:p.Pro42= | |
| ENST00000372940.3:c.125C= (MRPS16) | ENSP00000362031.3:p.Pro42= | |
| ENST00000372945.7:c.125C= (MRPS16) | ENSP00000362036.3:p.Pro42= | |
| ENST00000471251.5:n.258C= (MRPS16) | ||
| ENST00000473427.1:n.215C= (MRPS16) | ||
| ENST00000479005.1:n.282C= (MRPS16) | ||
| NM_016065.3:c.125C= (MRPS16) | NP_057149.1:p.Pro42= | |
| NR_038373.1:n.175+3462G= (DNAJC9-AS1) | ||
| XR_946059.1:n.120+171G= | ||
| NM_016065.4:c.125C= (MRPS16) MANE Select | NP_057149.1:p.Pro42= |