Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.73249425A>T , CM000672.2:g.73249425A>T | GRCh38 |
| NC_000010.10:g.75009183A>T , CM000672.1:g.75009183A>T | GRCh37 |
| NC_000010.9:g.74679189A>T | NCBI36 |
| NG_008096.1:g.8269T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372945.8:c.*1427T>A (MRPS16) MANE Select | ENSP00000362036.3:n.*1427T>A | |
| ENST00000372940.3:c.275-107T>A (MRPS16) | ENSP00000362031.3:n.275-107T>A | |
| ENST00000372945.7:c.*1427T>A (MRPS16) | ENSP00000362036.3:n.*1427T>A | |
| ENST00000479005.1:n.1998T>A (MRPS16) | ||
| NM_016065.3:c.*1427T>A (MRPS16) | NP_057149.1:n.*1427T>A | |
| NR_038373.1:n.175+975A>T (DNAJC9-AS1) | ||
| NM_016065.4:c.*1427T>A (MRPS16) MANE Select | NP_057149.1:n.*1427T>A |