HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734209_4734214delinsACAAAG , CM000679.2:g.4734209_4734214delinsACAAAG | GRCh38 |
NC_000017.10:g.4637504_4637509delinsACAAAG , CM000679.1:g.4637504_4637509delinsACAAAG | GRCh37 |
NC_000017.9:g.4584253_4584258delinsACAAAG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*289_*294delinsCTTTGT MANE Select | ENSP00000293778.7:n.*289_*294delinsCTTTGT | |
ENST00000293778.10:c.*289_*294delinsCTTTGT | ENSP00000293778.6:n.*289_*294delinsCTTTGT | |
ENST00000576153.5:n.845_850delinsCTTTGT | ||
NM_022059.3:c.*289_*294delinsCTTTGT | NP_071342.2:n.*289_*294delinsCTTTGT | |
NM_022059.4:c.*289_*294delinsCTTTGT | NP_071342.2:n.*289_*294delinsCTTTGT | |
NM_001386809.1:c.*289_*294delinsCTTTGT MANE Select | NP_001373738.1:n.*289_*294delinsCTTTGT |