Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42911210del , CM000679.2:g.42911210del | GRCh38 |
| NC_000017.10:g.41063227del , CM000679.1:g.41063227del | GRCh37 |
| NC_000017.9:g.38316753del | NCBI36 |
| NG_011808.1:g.15413del , LRG_147:g.15413del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000253801.7:c.858del MANE Select | ENSP00000253801.1:p.Lys287AsnfsTer14 | |
| ENST00000253801.6:c.858del | ENSP00000253801.1:p.Lys287AsnfsTer14 | |
| ENST00000585489.1:c.*250del | ENSP00000466202.1:n.*250del | |
| ENST00000592383.5:c.*250del | ENSP00000465958.1:n.*250del | |
| NM_000151.3:c.858del | NP_000142.2:p.Lys287AsnfsTer14 | |
| NM_001270397.1:c.*250del | NP_001257326.1:n.*250del | |
| NM_000151.4:c.858del MANE Select | NP_000142.2:p.Lys287AsnfsTer14 | |
| NM_001270397.2:c.*250del | NP_001257326.1:n.*250del |