Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86739793_86739800del , CM000670.2:g.86739793_86739800del | GRCh38 |
| NC_000008.10:g.87752021_87752028del , CM000670.1:g.87752021_87752028del | GRCh37 |
| NC_000008.9:g.87821137_87821144del | NCBI36 |
| NG_016980.1:g.8877_8884del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.130-63_130-56del MANE Select | ENSP00000316605.5:n.130-63_130-56del | |
| ENST00000681746.1:c.130-63_130-56del | ENSP00000505959.1:n.130-63_130-56del | |
| ENST00000320005.5:c.130-63_130-56del | ENSP00000316605.5:n.130-63_130-56del | |
| ENST00000519777.1:n.112-63_112-56del | ||
| NM_019098.4:c.130-63_130-56del | NP_061971.3:n.130-63_130-56del | |
| NM_019098.5:c.130-63_130-56del MANE Select | NP_061971.3:n.130-63_130-56del |