Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94008277del , CM000663.2:g.94008277del | GRCh38 |
| NC_000001.10:g.94473833del , CM000663.1:g.94473833del | GRCh37 |
| NC_000001.9:g.94246421del | NCBI36 |
| NG_009073.1:g.117875del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370225.4:c.5858del MANE Select | ENSP00000359245.3:p.Pro1953GlnfsTer21 | |
| ENST00000370225.3:c.5858del | ENSP00000359245.3:p.Pro1953GlnfsTer21 | |
| ENST00000465352.1:n.274del | ||
| ENST00000536513.5:c.2234del | ENSP00000439707.2:p.Pro745GlnfsTer21 | |
| NM_000350.2:c.5858del | NP_000341.2:p.Pro1953GlnfsTer21 | |
| NM_000350.3:c.5858del MANE Select | NP_000341.2:p.Pro1953GlnfsTer21 |