HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734225_4734228del , CM000679.2:g.4734225_4734228del | GRCh38 |
NC_000017.10:g.4637520_4637523del , CM000679.1:g.4637520_4637523del | GRCh37 |
NC_000017.9:g.4584269_4584272del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*278_*281del MANE Select | ENSP00000293778.7:n.*278_*281del | |
ENST00000293778.10:c.*278_*281del | ENSP00000293778.6:n.*278_*281del | |
ENST00000576153.5:n.834_837del | ||
NM_022059.3:c.*278_*281del | NP_071342.2:n.*278_*281del | |
NM_022059.4:c.*278_*281del | NP_071342.2:n.*278_*281del | |
NM_001386809.1:c.*278_*281del MANE Select | NP_001373738.1:n.*278_*281del |