Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94947216_94947218del , CM000672.2:g.94947216_94947218del | GRCh38 |
| NC_000010.10:g.96706973_96706975del , CM000672.1:g.96706973_96706975del | GRCh37 |
| NC_000010.9:g.96696963_96696965del | NCBI36 |
| NG_008385.1:g.13559_13561del | |
| NG_008385.2:g.14059_14061del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260682.8:c.482-563_482-561del MANE Select | ENSP00000260682.6:n.482-563_482-561del | |
| ENST00000643112.1:c.482-563_482-561del | ENSP00000496202.1:n.482-563_482-561del | |
| ENST00000645207.1:n.635-563_635-561del | ||
| ENST00000260682.6:c.482-563_482-561del | ENSP00000260682.6:n.482-563_482-561del | |
| ENST00000473496.1:n.253-563_253-561del | ||
| NM_000771.3:c.482-563_482-561del | NP_000762.2:n.482-563_482-561del | |
| NM_000771.4:c.482-563_482-561del MANE Select | NP_000762.2:n.482-563_482-561del |