Linked Data
MyVariant Identifiers:
chr17:g.4631566del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4631566del , CM000679.2:g.4631566del | GRCh38 |
| NC_000017.10:g.4534861del , CM000679.1:g.4534861del | GRCh37 |
| NC_000017.9:g.4481610del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000293761.8:c.*34del MANE Select | ENSP00000293761.3:n.*34del | |
| ENST00000570836.6:c.*34del | ENSP00000458832.1:n.*34del | |
| ENST00000293761.7:c.*34del | ENSP00000293761.3:n.*34del | |
| ENST00000570836.5:c.*34del | ENSP00000458832.1:n.*34del | |
| ENST00000574640.1:c.*34del | ENSP00000460483.1:n.*34del | |
| NM_001140.3:c.*34del | NP_001131.3:n.*34del | |
| NM_001140.4:c.*34del | NP_001131.3:n.*34del | |
| NM_001140.5:c.*34del MANE Select | NP_001131.3:n.*34del |