Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.27924575del , CM000675.2:g.27924575del | GRCh38 |
| NC_000013.10:g.28498712del , CM000675.1:g.28498712del | GRCh37 |
| NC_000013.9:g.27396712del | NCBI36 |
| NG_008183.1:g.9545del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381033.5:c.726del MANE Select | ENSP00000370421.4:p.Gly245GlufsTer? | |
| ENST00000381033.4:c.726del | ENSP00000370421.4:p.Gly245GlufsTer? | |
| NM_000209.3:c.726del | NP_000200.1:p.Gly245GlufsTer? | |
| NM_000209.4:c.726del MANE Select | NP_000200.1:p.Gly245GlufsTer? |