Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116832898del , CM000673.2:g.116832898del | GRCh38 |
| NC_000011.9:g.116703614del , CM000673.1:g.116703614del | GRCh37 |
| NC_000011.8:g.116208824del | NCBI36 |
| NG_008949.1:g.7991del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000227667.8:c.*14del MANE Select | ENSP00000227667.2:n.*14del | |
| ENST00000227667.7:c.*14del | ENSP00000227667.2:n.*14del | |
| ENST00000375345.3:c.*14del | ENSP00000364494.1:n.*14del | |
| ENST00000630701.1:c.368del | ENSP00000486182.1:n.368del | |
| NM_000040.1:c.*14del | NP_000031.1:n.*14del | |
| NM_000040.2:c.*14del | NP_000031.1:n.*14del | |
| NM_000040.3:c.*14del MANE Select | NP_000031.1:n.*14del |