Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52492479del , CM000674.2:g.52492479del | GRCh38 |
| NC_000012.11:g.52886263del , CM000674.1:g.52886263del | GRCh37 |
| NC_000012.10:g.51172530del | NCBI36 |
| NG_008298.1:g.5923del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000330722.7:c.540+174del MANE Select | ENSP00000369317.3:n.540+174del | |
| ENST00000330722.6:c.540+174del | ENSP00000369317.3:n.540+174del | |
| ENST00000549898.5:n.61+174del | ||
| NM_005554.3:c.540+174del | NP_005545.1:n.540+174del | |
| NM_005554.4:c.540+174del MANE Select | NP_005545.1:n.540+174del |