Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37966152_37966157del , CM000670.2:g.37966152_37966157del | GRCh38 |
| NC_000008.10:g.37823670_37823675del , CM000670.1:g.37823670_37823675del | GRCh37 |
| NC_000008.9:g.37942827_37942832del | NCBI36 |
| NG_011936.1:g.5510_5515del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000345060.5:c.313_318del MANE Select | ENSP00000343782.3:p.Leu105_Gly106del | |
| ENST00000520341.2:n.441_446del | ||
| ENST00000345060.4:c.313_318del | ENSP00000343782.3:p.Leu105_Gly106del | |
| ENST00000614635.1:c.313_318del | ENSP00000480325.1:p.Leu105_Gly106del | |
| NM_000025.2:c.313_318del | NP_000016.1:p.Leu105_Gly106del | |
| NM_000025.3:c.313_318del MANE Select | NP_000016.1:p.Leu105_Gly106del |