HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734131_4734132insCAAAA , CM000679.2:g.4734131_4734132insCAAAA | GRCh38 |
NC_000017.10:g.4637426_4637427insCAAAA , CM000679.1:g.4637426_4637427insCAAAA | GRCh37 |
NC_000017.9:g.4584175_4584176insCAAAA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*371_*372insTTTTG MANE Select | ENSP00000293778.7:n.*371_*372insTTTTG | |
ENST00000293778.10:c.*371_*372insTTTTG | ENSP00000293778.6:n.*371_*372insTTTTG | |
ENST00000576153.5:n.927_928insTTTTG | ||
NM_022059.3:c.*371_*372insTTTTG | NP_071342.2:n.*371_*372insTTTTG | |
NM_022059.4:c.*371_*372insTTTTG | NP_071342.2:n.*371_*372insTTTTG | |
NM_001386809.1:c.*371_*372insTTTTG MANE Select | NP_001373738.1:n.*371_*372insTTTTG |