Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.86739764_86739774del , CM000670.2:g.86739764_86739774del | GRCh38 |
| NC_000008.10:g.87751992_87752002del , CM000670.1:g.87751992_87752002del | GRCh37 |
| NC_000008.9:g.87821108_87821118del | NCBI36 |
| NG_016980.1:g.8903_8913del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000320005.6:c.130-37_130-27del MANE Select | ENSP00000316605.5:n.130-37_130-27del | |
| ENST00000681746.1:c.130-37_130-27del | ENSP00000505959.1:n.130-37_130-27del | |
| ENST00000320005.5:c.130-37_130-27del | ENSP00000316605.5:n.130-37_130-27del | |
| ENST00000519777.1:n.112-37_112-27del | ||
| NM_019098.4:c.130-37_130-27del | NP_061971.3:n.130-37_130-27del | |
| NM_019098.5:c.130-37_130-27del MANE Select | NP_061971.3:n.130-37_130-27del |