Linked Data
gnomAD v4:
15-74755381-C-CA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74755381_74755382insA , CM000677.2:g.74755381_74755382insA | GRCh38 |
| NC_000015.9:g.75047722_75047723insA , CM000677.1:g.75047722_75047723insA | GRCh37 |
| NC_000015.8:g.72834775_72834776insA | NCBI36 |
| NG_008431.1:g.37840_37841insA | |
| NG_008431.2:g.37840_37841insA | |
| NG_061543.1:g.11537_11538insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.*293_*294insA MANE Select | ENSP00000342007.4:n.*293_*294insA | |
| ENST00000343932.4:c.*293_*294insA | ENSP00000342007.4:n.*293_*294insA | |
| NM_000761.4:c.*293_*294insA | NP_000752.2:n.*293_*294insA | |
| NM_000761.5:c.*293_*294insA MANE Select | NP_000752.2:n.*293_*294insA |