Linked Data
gnomAD v4:
1-160881829-A-ATG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.160881830_160881831insGT , CM000663.2:g.160881830_160881831insGT | GRCh38 |
| NC_000001.10:g.160851620_160851621insGT , CM000663.1:g.160851620_160851621insGT | GRCh37 |
| NC_000001.9:g.159118244_159118245insGT | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000326245.4:c.405+127_405+128insCA MANE Select | ENSP00000323587.3:n.405+127_405+128insCA | |
| ENST00000326245.3:c.405+127_405+128insCA | ENSP00000323587.3:n.405+127_405+128insCA | |
| ENST00000464077.1:n.339+127_339+128insCA | ||
| NM_017625.2:c.405+127_405+128insCA | NP_060095.2:n.405+127_405+128insCA | |
| NM_017625.3:c.405+127_405+128insCA MANE Select | NP_060095.2:n.405+127_405+128insCA |