Linked Data
gnomAD v4:
17-41584065-C-CTA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584066_41584067insAT , CM000679.2:g.41584066_41584067insAT | GRCh38 |
| NC_000017.10:g.39740318_39740319insAT , CM000679.1:g.39740318_39740319insAT | GRCh37 |
| NC_000017.9:g.36993844_36993845insAT | NCBI36 |
| NG_008624.1:g.7830_7831insTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-145_766-144insTA MANE Select | ENSP00000167586.6:n.766-145_766-144insTA | |
| ENST00000167586.6:c.766-145_766-144insTA | ENSP00000167586.6:n.766-145_766-144insTA | |
| ENST00000476662.1:n.216-145_216-144insTA | ||
| NM_000526.4:c.766-145_766-144insTA | NP_000517.2:n.766-145_766-144insTA | |
| NM_000526.5:c.766-145_766-144insTA MANE Select | NP_000517.3:n.766-145_766-144insTA |