Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5226985_5226986del , CM000673.2:g.5226985_5226986del | GRCh38 |
| NC_000011.9:g.5248215_5248216del , CM000673.1:g.5248215_5248216del | GRCh37 |
| NC_000011.8:g.5204791_5204792del | NCBI36 |
| NG_000007.3:g.70630_70631del | |
| NG_059281.1:g.5086_5087del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.36_37del | ENSP00000494175.1:p.Thr13CysfsTer10 | |
| ENST00000335295.4:c.36_37del MANE Select | ENSP00000333994.3:p.Thr13CysfsTer10 | |
| ENST00000380315.2:c.36_37del | ENSP00000369671.2:p.Thr13CysfsTer10 | |
| ENST00000485743.1:n.87_88del | ||
| ENST00000633227.1:c.36_37del | ENSP00000488004.1:p.Thr13CysfsTer10 | |
| NM_000518.4:c.36_37del | NP_000509.1:p.Thr13CysfsTer10 | |
| NM_000518.5:c.36_37del MANE Select | NP_000509.1:p.Thr13CysfsTer10 |