Linked Data
gnomAD v4:
15-38252896-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.38252901del , CM000677.2:g.38252901del | GRCh38 |
| NC_000015.9:g.38545102del , CM000677.1:g.38545102del | GRCh37 |
| NC_000015.8:g.36332394del | NCBI36 |
| NG_008980.1:g.5051del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000299084.9:c.-285del MANE Select | ENSP00000299084.4:n.-285del | |
| ENST00000299084.8:c.-285del | ENSP00000299084.4:n.-285del | |
| ENST00000561205.1:n.54del | ||
| NM_152594.2:c.-285del | NP_689807.1:n.-285del | |
| XM_005254202.2:c.-285del | XP_005254259.1:n.-285del | |
| XM_005254203.3:c.-332del | XP_005254260.1:n.-332del | |
| XM_005254202.3:c.-285del | XP_005254259.1:n.-285del | |
| XR_001751484.1:n.87+670del | ||
| NM_152594.3:c.-285del MANE Select | NP_689807.1:n.-285del |