Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.44118515del , CM000682.2:g.44118515del | GRCh38 |
| NC_000020.10:g.42747155del , CM000682.1:g.42747155del | GRCh37 |
| NC_000020.9:g.42180569del | NCBI36 |
| NG_031867.1:g.74064del , LRG_394:g.74064del |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_020433.5:c.1278del MANE Select | NP_065166.2:p.Tyr427ThrfsTer? |
| ENST00000372980.4:c.1278del MANE Select | ENSP00000362071.3:p.Tyr427ThrfsTer? |
| NM_020433.4:c.1278del , LRG_394t1:c.1278del | NP_065166.2:p.Tyr427ThrfsTer? |
| ENST00000372980.3:c.1278del | ENSP00000362071.3:p.Tyr427ThrfsTer? |
| XM_006723832.2:c.1278del | XP_006723895.1:p.Tyr427ThrfsTer? |