Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.49457947_49457953del , CM000668.2:g.49457947_49457953del | GRCh38 |
| NC_000006.11:g.49425660_49425666del , CM000668.1:g.49425660_49425666del | GRCh37 |
| NC_000006.10:g.49533619_49533625del | NCBI36 |
| NG_007100.1:g.10188_10194del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274813.4:c.492_498del MANE Select | ENSP00000274813.3:p.Ile164MetfsTer14 | |
| ENST00000274813.3:c.492_498del | ENSP00000274813.3:p.Ile164MetfsTer14 | |
| NM_000255.3:c.492_498del | NP_000246.2:p.Ile164MetfsTer14 | |
| XM_005249143.2:c.492_498del | XP_005249200.1:p.Ile164MetfsTer14 | |
| XM_005249143.3:c.492_498del | XP_005249200.1:p.Ile164MetfsTer14 | |
| NM_000255.4:c.492_498del MANE Select | NP_000246.2:p.Ile164MetfsTer14 |