| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52038258_52038259del , CM000666.2:g.52038258_52038259del | GRCh38 |
| NC_000004.11:g.52904424_52904425del , CM000666.1:g.52904424_52904425del | GRCh37 |
| NC_000004.10:g.52599181_52599182del | NCBI36 |
| NG_008891.1:g.5061_5062del , LRG_204:g.5061_5062del |
| HGVS | Amino-acid Change |
|---|---|
| NM_000232.5:c.1_2del MANE Select | NP_000223.1:p.Met1GlyfsTer23 |
| ENST00000381431.10:c.1_2del MANE Select | ENSP00000370839.6:p.Met1GlyfsTer23 |
| NM_000232.4:c.1_2del , LRG_204t1:c.1_2del | NP_000223.1:p.Met1GlyfsTer23 |
| ENST00000381431.9:c.1_2del | ENSP00000370839.5:p.Met1GlyfsTer23 |
| XM_011534403.1:c.1_2del | XP_011532705.1:p.Met1GlyfsTer27 |