Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.91950116_91950120del , CM000671.2:g.91950116_91950120del | GRCh38 |
| NC_000009.11:g.94712398_94712402del , CM000671.1:g.94712398_94712402del | GRCh37 |
| NC_000009.10:g.93752219_93752223del | NCBI36 |
| NG_008089.1:g.5043_5047del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375708.4:c.-157_-153del MANE Select | ENSP00000364860.3:n.-157_-153del | |
| ENST00000375708.3:c.-157_-153del | ENSP00000364860.3:n.-157_-153del | |
| NM_004560.3:c.-157_-153del | NP_004551.2:n.-157_-153del | |
| NM_001318204.1:c.-157_-153del | NP_001305133.1:n.-157_-153del | |
| XR_001746315.1:n.87_91del | ||
| NM_004560.4:c.-157_-153del MANE Select | NP_004551.2:n.-157_-153del | |
| NM_001318204.2:c.-157_-153del | NP_001305133.1:n.-157_-153del |