Linked Data
gnomAD v4:
17-41584031-CCTT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584034_41584036del , CM000679.2:g.41584034_41584036del | GRCh38 |
| NC_000017.10:g.39740286_39740288del , CM000679.1:g.39740286_39740288del | GRCh37 |
| NC_000017.9:g.36993812_36993814del | NCBI36 |
| NG_008624.1:g.7862_7864del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-113_766-111del MANE Select | ENSP00000167586.6:n.766-113_766-111del | |
| ENST00000167586.6:c.766-113_766-111del | ENSP00000167586.6:n.766-113_766-111del | |
| ENST00000476662.1:n.216-113_216-111del | ||
| NM_000526.4:c.766-113_766-111del | NP_000517.2:n.766-113_766-111del | |
| NM_000526.5:c.766-113_766-111del MANE Select | NP_000517.3:n.766-113_766-111del |