Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652453_171652459del , CM000663.2:g.171652453_171652459del | GRCh38 |
| NC_000001.10:g.171621593_171621599del , CM000663.1:g.171621593_171621599del | GRCh37 |
| NC_000001.9:g.169888216_169888222del | NCBI36 |
| NG_008859.1:g.5175_5181del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.153_159del MANE Select | ENSP00000037502.5:p.Phe51LeufsTer? | |
| ENST00000638471.1:c.130+23_130+29del | ENSP00000491206.1:n.130+23_130+29del | |
| ENST00000037502.10:c.153_159del | ENSP00000037502.5:p.Phe51LeufsTer? | |
| ENST00000614688.1:c.153_159del | ENSP00000478680.1:p.Phe51LeufsTer? | |
| NM_000261.1:c.153_159del | NP_000252.1:p.Phe51LeufsTer? | |
| NM_000261.2:c.153_159del MANE Select | NP_000252.1:p.Phe51LeufsTer? |