Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.10612928_10612939del , CM000670.2:g.10612928_10612939del | GRCh38 |
| NC_000008.10:g.10470438_10470449del , CM000670.1:g.10470438_10470449del | GRCh37 |
| NC_000008.9:g.10507848_10507859del | NCBI36 |
| NG_028035.1:g.47176_47187del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382483.4:c.1166_1177del MANE Select | ENSP00000371923.3:p.Val389_Arg392del | |
| ENST00000382483.3:c.1166_1177del | ENSP00000371923.3:p.Val389_Arg392del | |
| NM_178857.5:c.1166_1177del | NP_849188.4:p.Val389_Arg392del | |
| NM_178857.6:c.1166_1177del MANE Select | NP_849188.4:p.Val389_Arg392del |