Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.5225702del , CM000673.2:g.5225702del | GRCh38 |
| NC_000011.9:g.5246932del , CM000673.1:g.5246932del | GRCh37 |
| NC_000011.8:g.5203508del | NCBI36 |
| NG_000007.3:g.71914del | |
| NG_059281.1:g.6370del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000647020.1:c.340del | ENSP00000494175.1:p.Val114CysfsTer? | |
| ENST00000335295.4:c.340del MANE Select | ENSP00000333994.3:p.Val114CysfsTer? | |
| ENST00000475226.1:n.272del | ||
| ENST00000633227.1:c.*156del | ENSP00000488004.1:n.*156del | |
| NM_000518.4:c.340del | NP_000509.1:p.Val114CysfsTer? | |
| NM_000518.5:c.340del MANE Select | NP_000509.1:p.Val114CysfsTer? |