Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138945397del , CM000665.2:g.138945397del | GRCh38 |
| NC_000003.11:g.138664239del , CM000665.1:g.138664239del | GRCh37 |
| NC_000003.10:g.140146929del | NCBI36 |
| NG_012454.1:g.6744del | |
| NG_029796.1:g.3164del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.*195del MANE Select | ENSP00000497217.1:n.*195del | |
| ENST00000330315.3:c.*195del | ENSP00000333188.3:n.*195del | |
| NM_023067.3:c.*195del | NP_075555.1:n.*195del | |
| NM_023067.4:c.*195del MANE Select | NP_075555.1:n.*195del |