HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186086039_186086040insA , CM000666.2:g.186086039_186086040insA | GRCh38 |
NC_000004.11:g.187007193_187007194insA , CM000666.1:g.187007193_187007194insA | GRCh37 |
NC_000004.10:g.187244187_187244188insA | NCBI36 |
NG_007278.1:g.21885_21886insA , LRG_117:g.21885_21886insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3433_*3434insA | ENSP00000513675.1:n.*3433_*3434insA | |
ENST00000698353.1:n.3756_3757insA | ||
ENST00000698354.1:c.*1166_*1167insA | ENSP00000513676.1:n.*1166_*1167insA | |
ENST00000296795.8:c.*1166_*1167insA MANE Select | ENSP00000296795.3:n.*1166_*1167insA | |
ENST00000296795.7:c.*1166_*1167insA | ENSP00000296795.2:n.*1166_*1167insA | |
NM_003265.3:c.*1166_*1167insA MANE Select | NP_003256.1:n.*1166_*1167insA |