Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.55039917del , CM000663.2:g.55039917del | GRCh38 |
| NC_000001.10:g.55505590del , CM000663.1:g.55505590del | GRCh37 |
| NC_000001.9:g.55278178del | NCBI36 |
| NG_009061.1:g.5371del , LRG_275:g.5371del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673913.2:c.80del | ENSP00000501161.2:p.Gly27AlafsTer17 | |
| ENST00000710286.1:c.437del | ENSP00000518176.1:p.Gly146AlafsTer17 | |
| ENST00000673726.1:c.80del | ENSP00000501004.1:p.Gly27AlafsTer17 | |
| ENST00000302118.5:c.80del MANE Select | ENSP00000303208.5:p.Gly27AlafsTer17 | |
| NM_174936.3:c.80del , LRG_275t1:c.80del | NP_777596.2:p.Gly27AlafsTer17 | |
| NM_174936.4:c.80del MANE Select | NP_777596.2:p.Gly27AlafsTer17 |