Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176093634_176093637del , CM000664.2:g.176093634_176093637del | GRCh38 |
| NC_000002.11:g.176958362_176958365del , CM000664.1:g.176958362_176958365del | GRCh37 |
| NC_000002.10:g.176666608_176666611del | NCBI36 |
| NG_008137.1:g.5831_5834del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392539.4:c.744_747del MANE Select | ENSP00000376322.3:p.Gln248HisfsTer17 | |
| ENST00000392539.3:c.744_747del | ENSP00000376322.3:p.Gln248HisfsTer17 | |
| NM_000523.3:c.744_747del | NP_000514.2:p.Gln248HisfsTer17 | |
| XM_011511068.1:c.725-846_725-843del | XP_011509370.1:n.725-846_725-843del | |
| XM_011511068.2:c.725-846_725-843del | XP_011509370.1:n.725-846_725-843del | |
| NM_000523.4:c.744_747del MANE Select | NP_000514.2:p.Gln248HisfsTer17 |