Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.100189370del , CM000663.2:g.100189370del | GRCh38 |
| NC_000001.10:g.100654926del , CM000663.1:g.100654926del | GRCh37 |
| NC_000001.9:g.100427514del | NCBI36 |
| NG_011852.2:g.65502del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001918.5:c.*6903del MANE Select | NP_001909.4:n.*6903del |
| ENST00000370132.8:c.*6903del MANE Select | ENSP00000359151.3:n.*6903del |
| NM_001399969.1:c.*6903del | NP_001386898.1:n.*6903del |
| NM_001399972.1:c.*6903del | NP_001386901.1:n.*6903del |
| NM_001918.3:c.*6903del | NP_001909.3:n.*6903del |
| NM_001918.4:c.*6903del | NP_001909.3:n.*6903del |
| NR_174363.1:n.8184del | |
| NR_174364.1:n.8525del | |
| NR_174365.1:n.8149del | |
| NR_174366.1:n.8451del |