HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149884693_149884694insTGAA , CM000663.2:g.149884693_149884694insTGAA | GRCh38 |
NC_000001.10:g.149856243_149856244insTGAA , CM000663.1:g.149856243_149856244insTGAA | GRCh37 |
NC_000001.9:g.148122867_148122868insTGAA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369155.4:c.*1566_*1567insTTCA MANE Select | ENSP00000358151.2:n.*1566_*1567insTTCA | |
ENST00000369155.3:c.*1566_*1567insTTCA | ENSP00000358151.2:n.*1566_*1567insTTCA | |
ENST00000369160.3:c.377+1570_377+1571insTTCA | ENSP00000375736.2:n.377+1570_377+1571insTTCA | |
NM_003528.2:c.*1566_*1567insTTCA | NP_003519.1:n.*1566_*1567insTTCA | |
NM_003528.3:c.*1566_*1567insTTCA MANE Select | NP_003519.1:n.*1566_*1567insTTCA |