Linked Data
gnomAD v4:
14-24258818-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.24258821del , CM000676.2:g.24258821del | GRCh38 |
| NC_000014.8:g.24728027del , CM000676.1:g.24728027del | GRCh37 |
| NC_000014.7:g.23797867del | NCBI36 |
| NG_007150.1:g.9348del | |
| NG_007150.2:g.9348del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000206765.11:c.1160-146del MANE Select | ENSP00000206765.6:n.1160-146del | |
| ENST00000206765.10:c.1160-146del | ENSP00000206765.6:n.1160-146del | |
| ENST00000544573.5:c.-28-431del | ENSP00000439446.1:n.-28-431del | |
| ENST00000559136.1:c.233-146del | ENSP00000453337.1:n.233-146del | |
| NM_000359.2:c.1160-146del | NP_000350.1:n.1160-146del | |
| NM_000359.3:c.1160-146del MANE Select | NP_000350.1:n.1160-146del |