Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.114044185del , CM000672.2:g.114044185del | GRCh38 |
| NC_000010.10:g.115803944del , CM000672.1:g.115803944del | GRCh37 |
| NC_000010.9:g.115793934del | NCBI36 |
| NG_012187.1:g.5139del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369295.4:c.53del MANE Select | ENSP00000358301.2:p.Ser18TrpfsTer? | |
| ENST00000369295.3:c.53del | ENSP00000358301.2:p.Ser18TrpfsTer? | |
| NM_000684.2:c.53del | NP_000675.1:p.Ser18TrpfsTer? | |
| NM_000684.3:c.53del MANE Select | NP_000675.1:p.Ser18TrpfsTer? |