Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155022615del , CM000685.2:g.155022615del | GRCh38 |
| NC_000023.10:g.154250890del , CM000685.1:g.154250890del | GRCh37 |
| NC_000023.9:g.153904084del | NCBI36 |
| NG_011403.1:g.5111del | |
| NG_011403.2:g.5111del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.-61del MANE Select | ENSP00000353393.4:n.-61del | |
| ENST00000647125.1:c.-61del | ENSP00000496062.1:n.-61del | |
| ENST00000360256.8:c.-61del | ENSP00000353393.4:n.-61del | |
| ENST00000423959.5:c.38+4167del | ENSP00000409446.1:n.38+4167del | |
| ENST00000453950.1:c.39-117del | ENSP00000389153.1:n.39-117del | |
| NM_000132.3:c.-61del | NP_000123.1:n.-61del | |
| XM_011531126.1:c.38+4167del | XP_011529428.1:n.38+4167del | |
| NM_000132.4:c.-61del MANE Select | NP_000123.1:n.-61del |