Linked Data
gnomAD v4:
6-151618206-AAATTC-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151618207_151618211del , CM000668.2:g.151618207_151618211del | GRCh38 |
| NC_000006.11:g.151939342_151939346del , CM000668.1:g.151939342_151939346del | GRCh37 |
| NC_000006.10:g.151981035_151981039del | NCBI36 |
| NG_021198.1:g.129168_129172del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000239374.8:c.*60_*64del MANE Select | ENSP00000239374.6:n.*60_*64del | |
| ENST00000239374.7:c.*60_*64del | ENSP00000239374.6:n.*60_*64del | |
| NM_025059.3:c.*60_*64del | NP_079335.2:n.*60_*64del | |
| XM_011536147.1:c.*60_*64del | XP_011534449.1:n.*60_*64del | |
| XM_011536148.1:c.*60_*64del | XP_011534450.1:n.*60_*64del | |
| XM_011536147.2:c.*60_*64del | XP_011534449.1:n.*60_*64del | |
| XM_011536148.2:c.*60_*64del | XP_011534450.1:n.*60_*64del | |
| NM_025059.4:c.*60_*64del MANE Select | NP_079335.2:n.*60_*64del |