Linked Data
gnomAD v4:
17-41584070-T-TCTA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.41584070_41584071insCTA , CM000679.2:g.41584070_41584071insCTA | GRCh38 |
| NC_000017.10:g.39740322_39740323insCTA , CM000679.1:g.39740322_39740323insCTA | GRCh37 |
| NC_000017.9:g.36993848_36993849insCTA | NCBI36 |
| NG_008624.1:g.7825_7826insTAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000167586.7:c.766-150_766-149insTAG MANE Select | ENSP00000167586.6:n.766-150_766-149insTAG | |
| ENST00000167586.6:c.766-150_766-149insTAG | ENSP00000167586.6:n.766-150_766-149insTAG | |
| ENST00000476662.1:n.216-150_216-149insTAG | ||
| NM_000526.4:c.766-150_766-149insTAG | NP_000517.2:n.766-150_766-149insTAG | |
| NM_000526.5:c.766-150_766-149insTAG MANE Select | NP_000517.3:n.766-150_766-149insTAG |