Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44289743del , CM000683.2:g.44289743del | GRCh38 |
| NC_000021.8:g.45709626del , CM000683.1:g.45709626del | GRCh37 |
| NC_000021.7:g.44534054del | NCBI36 |
| NG_009556.1:g.8864del , LRG_18:g.8864del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000291582.6:c.739del MANE Select | ENSP00000291582.5:p.Arg247AlafsTer? | |
| ENST00000291582.5:c.739del | ENSP00000291582.5:p.Arg247AlafsTer? | |
| ENST00000527919.5:n.1472del | ||
| ENST00000530812.5:n.2489del | ||
| NM_000383.3:c.739del | NP_000374.1:p.Arg247AlafsTer? | |
| XM_011529551.1:c.739del | XP_011527853.1:p.Arg247AlafsTer? | |
| NM_000383.4:c.739del MANE Select | NP_000374.1:p.Arg247AlafsTer? |