Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68431149del , CM000663.2:g.68431149del | GRCh38 |
| NC_000001.10:g.68896832del , CM000663.1:g.68896832del | GRCh37 |
| NC_000001.9:g.68669420del | NCBI36 |
| NG_008472.1:g.23811del | |
| NG_008472.2:g.23811del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000262340.6:c.1366del MANE Select | ENSP00000262340.5:p.Glu456LysfsTer30 | |
| ENST00000262340.5:c.1366del | ENSP00000262340.5:p.Glu456LysfsTer30 | |
| NM_000329.2:c.1366del | NP_000320.1:p.Glu456LysfsTer30 | |
| XM_017002027.1:c.1090del | XP_016857516.1:p.Glu364LysfsTer30 | |
| NM_000329.3:c.1366del MANE Select | NP_000320.1:p.Glu456LysfsTer30 |