Linked Data
gnomAD v4:
17-42536309-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42536311del , CM000679.2:g.42536311del | GRCh38 |
| NC_000017.10:g.40688329del , CM000679.1:g.40688329del | GRCh37 |
| NC_000017.9:g.37941855del | NCBI36 |
| NG_011552.1:g.5379del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000225927.7:c.39del MANE Select | ENSP00000225927.1:p.Leu14SerfsTer? | |
| ENST00000225927.6:c.39del | ENSP00000225927.1:p.Leu14SerfsTer? | |
| NM_000263.3:c.39del | NP_000254.2:p.Leu14SerfsTer? | |
| XM_024450771.1:c.39del | XP_024306539.1:p.Leu14SerfsTer? | |
| NM_000263.4:c.39del MANE Select | NP_000254.2:p.Leu14SerfsTer? |