Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.68839650del , CM000685.2:g.68839650del | GRCh38 |
| NC_000023.10:g.68059493del , CM000685.1:g.68059493del | GRCh37 |
| NC_000023.9:g.67976218del | NCBI36 |
| NG_008887.1:g.15654del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000204961.5:c.407-14del MANE Select | ENSP00000204961.4:n.407-14del | |
| ENST00000204961.4:c.407-14del | ENSP00000204961.4:n.407-14del | |
| NM_004429.4:c.407-14del | NP_004420.1:n.407-14del | |
| NM_004429.5:c.407-14del MANE Select | NP_004420.1:n.407-14del |