Linked Data
gnomAD v4:
17-41584053-C-CAA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584053_41584054insAA , CM000679.2:g.41584053_41584054insAA | GRCh38 |
| NC_000017.10:g.39740305_39740306insAA , CM000679.1:g.39740305_39740306insAA | GRCh37 |
| NC_000017.9:g.36993831_36993832insAA | NCBI36 |
| NG_008624.1:g.7842_7843insTT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-133_766-132insTT MANE Select | ENSP00000167586.6:n.766-133_766-132insTT | |
| ENST00000167586.6:c.766-133_766-132insTT | ENSP00000167586.6:n.766-133_766-132insTT | |
| ENST00000476662.1:n.216-133_216-132insTT | ||
| NM_000526.4:c.766-133_766-132insTT | NP_000517.2:n.766-133_766-132insTT | |
| NM_000526.5:c.766-133_766-132insTT MANE Select | NP_000517.3:n.766-133_766-132insTT |