Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7533802del , CM000681.2:g.7533802del | GRCh38 |
| NC_000019.9:g.7598688del , CM000681.1:g.7598688del | GRCh37 |
| NC_000019.8:g.7504688del | NCBI36 |
| NG_013374.1:g.4651del | |
| NG_015806.1:g.16193del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.*7del MANE Select | ENSP00000264079.5:n.*7del | |
| ENST00000264079.10:c.*7del | ENSP00000264079.5:n.*7del | |
| ENST00000394321.9:n.2065del | ||
| ENST00000599334.1:c.478del | ||
| ENST00000601870.1:c.103del | ||
| ENST00000602227.1:n.304del | ||
| NM_020533.2:c.*7del | NP_065394.1:n.*7del | |
| NM_020533.3:c.*7del MANE Select | NP_065394.1:n.*7del |