HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149926095_149926098delinsTTTA , CM000663.2:g.149926095_149926098delinsTTTA | GRCh38 |
NC_000001.10:g.149897987_149897990delinsTTTA , CM000663.1:g.149897987_149897990delinsTTTA | GRCh37 |
NC_000001.9:g.148164611_148164614delinsTTTA | NCBI36 |
NG_032777.1:g.7155_7158delinsTAAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.707-56_707-53delinsTAAA MANE Select | ENSP00000271628.8:n.707-56_707-53delinsTAAA | |
ENST00000271628.8:c.707-56_707-53delinsTAAA | ENSP00000271628.8:n.707-56_707-53delinsTAAA | |
NM_005850.4:c.707-56_707-53delinsTAAA | NP_005841.1:n.707-56_707-53delinsTAAA | |
NM_005850.5:c.707-56_707-53delinsTAAA MANE Select | NP_005841.1:n.707-56_707-53delinsTAAA |