Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.73251958T>A , CM000672.2:g.73251958T>A | GRCh38 |
| NC_000010.10:g.75011716T>A , CM000672.1:g.75011716T>A | GRCh37 |
| NC_000010.9:g.74681722T>A | NCBI36 |
| NG_008096.1:g.5736A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372945.8:c.79A>T (MRPS16) MANE Select | ENSP00000362036.3:p.Thr27Ser | |
| ENST00000372940.3:c.79A>T (MRPS16) | ENSP00000362031.3:p.Thr27Ser | |
| ENST00000372945.7:c.79A>T (MRPS16) | ENSP00000362036.3:p.Thr27Ser | |
| ENST00000471251.5:n.212A>T (MRPS16) | ||
| ENST00000473427.1:n.169A>T (MRPS16) | ||
| ENST00000479005.1:n.236A>T (MRPS16) | ||
| NM_016065.3:c.79A>T (MRPS16) | NP_057149.1:p.Thr27Ser | |
| NR_038373.1:n.175+3508T>A (DNAJC9-AS1) | ||
| XR_946059.1:n.120+217T>A | ||
| NM_016065.4:c.79A>T (MRPS16) MANE Select | NP_057149.1:p.Thr27Ser |