Linked Data
gnomAD v4:
17-42909284-GT-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42909286del , CM000679.2:g.42909286del | GRCh38 |
| NC_000017.10:g.41061303del , CM000679.1:g.41061303del | GRCh37 |
| NC_000017.9:g.38314829del | NCBI36 |
| NG_011808.1:g.13489del , LRG_147:g.13489del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253801.7:c.447-17del MANE Select | ENSP00000253801.1:n.447-17del | |
| ENST00000253801.6:c.447-17del | ENSP00000253801.1:n.447-17del | |
| ENST00000585489.1:c.447-1629del | ENSP00000466202.1:n.447-1629del | |
| ENST00000592383.5:c.370-17del | ENSP00000465958.1:n.370-17del | |
| NM_000151.3:c.447-17del | NP_000142.2:n.447-17del | |
| NM_001270397.1:c.370-17del | NP_001257326.1:n.370-17del | |
| NM_000151.4:c.447-17del MANE Select | NP_000142.2:n.447-17del | |
| NM_001270397.2:c.370-17del | NP_001257326.1:n.370-17del |