Linked Data
gnomAD v4:
15-74755349-T-TAAA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.74755349_74755350insAAA , CM000677.2:g.74755349_74755350insAAA | GRCh38 |
| NC_000015.9:g.75047690_75047691insAAA , CM000677.1:g.75047690_75047691insAAA | GRCh37 |
| NC_000015.8:g.72834743_72834744insAAA | NCBI36 |
| NG_008431.1:g.37808_37809insAAA | |
| NG_008431.2:g.37808_37809insAAA | |
| NG_061543.1:g.11505_11506insAAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000343932.5:c.*261_*262insAAA MANE Select | ENSP00000342007.4:n.*261_*262insAAA | |
| ENST00000343932.4:c.*261_*262insAAA | ENSP00000342007.4:n.*261_*262insAAA | |
| NM_000761.4:c.*261_*262insAAA | NP_000752.2:n.*261_*262insAAA | |
| NM_000761.5:c.*261_*262insAAA MANE Select | NP_000752.2:n.*261_*262insAAA |