Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.19117124del , CM000669.2:g.19117124del | GRCh38 |
| NC_000007.13:g.19156747del , CM000669.1:g.19156747del | GRCh37 |
| NC_000007.12:g.19123272del | NCBI36 |
| NG_008114.1:g.5551del | |
| NG_008114.2:g.5551del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000242261.6:c.200del MANE Select | ENSP00000242261.5:p.Gly67AlafsTer? | |
| ENST00000242261.5:c.200del | ENSP00000242261.5:p.Gly67AlafsTer? | |
| NM_000474.3:c.200del | NP_000465.1:p.Gly67AlafsTer? | |
| XM_011515496.1:c.200del | XP_011513798.1:p.Gly67AlafsTer? | |
| NR_149001.1:n.551del | ||
| NM_000474.4:c.200del MANE Select | NP_000465.1:p.Gly67AlafsTer? | |
| NR_149001.2:n.515del |