Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.136687437del , CM000671.2:g.136687437del | GRCh38 |
| NC_000009.11:g.139581889del , CM000671.1:g.139581889del | GRCh37 |
| NC_000009.10:g.138701710del | NCBI36 |
| NG_008090.1:g.5024del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371696.7:c.-79del MANE Select | ENSP00000360761.2:n.-79del | |
| NM_001012727.1:c.-79del | NP_001012745.1:n.-79del | |
| NM_006412.3:c.-79del | NP_006403.2:n.-79del | |
| NM_006412.4:c.-79del MANE Select | NP_006403.2:n.-79del | |
| NM_001012727.2:c.-79del | NP_001012745.1:n.-79del |