Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94780410del , CM000672.2:g.94780410del | GRCh38 |
| NC_000010.10:g.96540167del , CM000672.1:g.96540167del | GRCh37 |
| NC_000010.9:g.96530157del | NCBI36 |
| NG_008384.2:g.22705del | |
| NG_008384.3:g.22730del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371321.9:c.482-89del MANE Select | ENSP00000360372.3:n.482-89del | |
| ENST00000645461.1:n.1535-89del | ||
| ENST00000371321.7:c.482-89del | ENSP00000360372.3:n.482-89del | |
| ENST00000464755.1:c.1245-89del | ENSP00000483243.1:n.1245-89del | |
| NM_000769.2:c.482-89del | NP_000760.1:n.482-89del | |
| NM_000769.4:c.482-89del MANE Select | NP_000760.1:n.482-89del |