Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21178461del , CM000674.2:g.21178461del | GRCh38 |
| NC_000012.11:g.21331395del , CM000674.1:g.21331395del | GRCh37 |
| NC_000012.10:g.21222662del | NCBI36 |
| NG_011745.1:g.52268del , LRG_1022:g.52268del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000256958.3:c.482-115del MANE Select | ENSP00000256958.2:n.482-115del | |
| ENST00000256958.2:c.482-115del | ENSP00000256958.2:n.482-115del | |
| NM_006446.4:c.482-115del , LRG_1022t1:c.482-115del | NP_006437.3:n.482-115del | |
| NM_006446.5:c.482-115del MANE Select | NP_006437.3:n.482-115del |