HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734204_4734209delinsTCAAAA , CM000679.2:g.4734204_4734209delinsTCAAAA | GRCh38 |
NC_000017.10:g.4637499_4637504delinsTCAAAA , CM000679.1:g.4637499_4637504delinsTCAAAA | GRCh37 |
NC_000017.9:g.4584248_4584253delinsTCAAAA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*294_*299delinsTTTTGA MANE Select | ENSP00000293778.7:n.*294_*299delinsTTTTGA | |
ENST00000293778.10:c.*294_*299delinsTTTTGA | ENSP00000293778.6:n.*294_*299delinsTTTTGA | |
ENST00000576153.5:n.850_855delinsTTTTGA | ||
NM_022059.3:c.*294_*299delinsTTTTGA | NP_071342.2:n.*294_*299delinsTTTTGA | |
NM_022059.4:c.*294_*299delinsTTTTGA | NP_071342.2:n.*294_*299delinsTTTTGA | |
NM_001386809.1:c.*294_*299delinsTTTTGA MANE Select | NP_001373738.1:n.*294_*299delinsTTTTGA |