Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154904822del , CM000685.2:g.154904822del | GRCh38 |
| NC_000023.10:g.154133097del , CM000685.1:g.154133097del | GRCh37 |
| NC_000023.9:g.153786291del | NCBI36 |
| NG_011403.1:g.122902del | |
| NG_011403.2:g.122902del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5575del MANE Select | ENSP00000353393.4:p.Asp1859MetfsTer12 | |
| ENST00000360256.8:c.5575del | ENSP00000353393.4:p.Asp1859MetfsTer12 | |
| NM_000132.3:c.5575del | NP_000123.1:p.Asp1859MetfsTer12 | |
| XM_011531126.1:c.5470del | XP_011529428.1:p.Asp1824MetfsTer12 | |
| NM_000132.4:c.5575del MANE Select | NP_000123.1:p.Asp1859MetfsTer12 |