Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38409006del , CM000685.2:g.38409006del | GRCh38 |
| NC_000023.10:g.38268259del , CM000685.1:g.38268259del | GRCh37 |
| NC_000023.9:g.38153203del | NCBI36 |
| NG_008471.1:g.61524del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.848del MANE Select | ENSP00000039007.4:p.Gly283ValfsTer6 | |
| ENST00000643344.1:c.*598del | ENSP00000496606.1:n.*598del | |
| ENST00000039007.4:c.848del | ENSP00000039007.4:p.Gly283ValfsTer6 | |
| ENST00000465127.1:c.172-257115del | ENSP00000417050.1:n.172-257115del | |
| NM_000531.5:c.848del | NP_000522.3:p.Gly283ValfsTer6 | |
| XM_017029556.1:c.848del | XP_016885045.1:p.Gly283ValfsTer6 | |
| NM_000531.6:c.848del MANE Select | NP_000522.3:p.Gly283ValfsTer6 |