Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.138946105del , CM000665.2:g.138946105del | GRCh38 |
| NC_000003.11:g.138664947del , CM000665.1:g.138664947del | GRCh37 |
| NC_000003.10:g.140147637del | NCBI36 |
| NG_012454.1:g.6036del | |
| NG_029796.1:g.3872del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000648323.1:c.618del MANE Select | ENSP00000497217.1:p.Pro207ArgfsTer? | |
| ENST00000330315.3:c.618del | ENSP00000333188.3:p.Pro207ArgfsTer? | |
| NM_023067.3:c.618del | NP_075555.1:p.Pro207ArgfsTer? | |
| NM_023067.4:c.618del MANE Select | NP_075555.1:p.Pro207ArgfsTer? |