Linked Data
ClinVar Variation Id:
2682164
ClinVar RCV Id:
RCV003479537
ERepo:
CA16020726/MONDO:0009861/006
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102912885del , CM000674.2:g.102912885del | GRCh38 |
| NC_000012.11:g.103306663del , CM000674.1:g.103306663del | GRCh37 |
| NC_000012.10:g.101830793del | NCBI36 |
| NG_008690.1:g.9719del | |
| NG_008690.2:g.50527del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.75del MANE Select | ENSP00000448059.1:p.Ile25MetfsTer13 | |
| ENST00000307000.7:c.60del | ENSP00000303500.2:p.Ile20MetfsTer13 | |
| ENST00000546844.1:c.75del | ENSP00000446658.1:p.Ile25MetfsTer13 | |
| ENST00000548677.2:n.162del | ||
| ENST00000549111.5:n.171del | ||
| ENST00000550978.6:c.59del | ||
| ENST00000551337.5:c.75del | ENSP00000447620.1:p.Ile25MetfsTer13 | |
| ENST00000551988.5:n.164del | ||
| ENST00000553106.5:c.75del | ENSP00000448059.1:p.Ile25MetfsTer13 | |
| ENST00000635500.1:n.43del | ||
| NM_000277.1:c.75del | NP_000268.1:p.Ile25MetfsTer13 | |
| XM_011538422.1:c.75del | XP_011536724.1:p.Ile25MetfsTer13 | |
| NM_000277.2:c.75del | NP_000268.1:p.Ile25MetfsTer13 | |
| NM_001354304.1:c.75del | NP_001341233.1:p.Ile25MetfsTer13 | |
| XM_017019370.2:c.75del | XP_016874859.1:p.Ile25MetfsTer13 | |
| NM_000277.3:c.75del MANE Select | NP_000268.1:p.Ile25MetfsTer13 | |
| NM_001354304.2:c.75del | NP_001341233.1:p.Ile25MetfsTer13 |