HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229431340_229431342del , CM000663.2:g.229431340_229431342del | GRCh38 |
NC_000001.10:g.229567087_229567089del , CM000663.1:g.229567087_229567089del | GRCh37 |
NC_000001.9:g.227633710_227633712del | NCBI36 |
NG_006672.1:g.7755_7757del , LRG_429:g.7755_7757del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.*157_*159del | ENSP00000355644.4:n.*157_*159del | |
ENST00000684723.1:c.*157_*159del | ENSP00000508084.1:n.*157_*159del | |
ENST00000366683.3:c.*157_*159del | ENSP00000355644.3:n.*157_*159del | |
ENST00000366684.7:c.*157_*159del MANE Select | ENSP00000355645.3:n.*157_*159del | |
NM_001100.3:c.*157_*159del , LRG_429t1:c.*157_*159del | NP_001091.1:n.*157_*159del | |
NM_001100.4:c.*157_*159del MANE Select | NP_001091.1:n.*157_*159del |