Linked Data
gnomAD v4:
15-89776766-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89776768del , CM000677.2:g.89776768del | GRCh38 |
| NC_000015.9:g.90319999del , CM000677.1:g.90319999del | GRCh37 |
| NC_000015.8:g.88121003del | NCBI36 |
| NG_008608.1:g.5411del | |
| NG_008608.2:g.21178del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341735.5:c.411del MANE Select | ENSP00000342392.3:p.Val138CysfsTer? | |
| ENST00000341735.3:c.411del | ENSP00000342392.3:p.Val138CysfsTer? | |
| ENST00000558723.1:n.39-1297del | ||
| ENST00000560219.2:c.31-1297del | ENSP00000452998.1:n.31-1297del | |
| NM_001039958.1:c.411del | NP_001035047.1:p.Val138CysfsTer? | |
| NM_001039958.2:c.411del MANE Select | NP_001035047.1:p.Val138CysfsTer? |