HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186086041_186086042insG , CM000666.2:g.186086041_186086042insG | GRCh38 |
NC_000004.11:g.187007195_187007196insG , CM000666.1:g.187007195_187007196insG | GRCh37 |
NC_000004.10:g.187244189_187244190insG | NCBI36 |
NG_007278.1:g.21887_21888insG , LRG_117:g.21887_21888insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3435_*3436insG | ENSP00000513675.1:n.*3435_*3436insG | |
ENST00000698353.1:n.3758_3759insG | ||
ENST00000698354.1:c.*1168_*1169insG | ENSP00000513676.1:n.*1168_*1169insG | |
ENST00000296795.8:c.*1168_*1169insG MANE Select | ENSP00000296795.3:n.*1168_*1169insG | |
ENST00000296795.7:c.*1168_*1169insG | ENSP00000296795.2:n.*1168_*1169insG | |
NM_003265.3:c.*1168_*1169insG MANE Select | NP_003256.1:n.*1168_*1169insG |