Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138946589del , CM000665.2:g.138946589del | GRCh38 |
| NC_000003.11:g.138665431del , CM000665.1:g.138665431del | GRCh37 |
| NC_000003.10:g.140148121del | NCBI36 |
| NG_012454.1:g.5555del | |
| NG_029796.1:g.4356del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000648323.1:c.137del MANE Select | ENSP00000497217.1:p.Pro46ArgfsTer? | |
| ENST00000330315.3:c.137del | ENSP00000333188.3:p.Pro46ArgfsTer? | |
| NM_023067.3:c.137del | NP_075555.1:p.Pro46ArgfsTer? | |
| NM_023067.4:c.137del MANE Select | NP_075555.1:p.Pro46ArgfsTer? |