HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160881743_160881744insTTTA , CM000663.2:g.160881743_160881744insTTTA | GRCh38 |
NC_000001.10:g.160851533_160851534insTTTA , CM000663.1:g.160851533_160851534insTTTA | GRCh37 |
NC_000001.9:g.159118157_159118158insTTTA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.405+213_405+214insTAAA MANE Select | ENSP00000323587.3:n.405+213_405+214insTAAA | |
ENST00000326245.3:c.405+213_405+214insTAAA | ENSP00000323587.3:n.405+213_405+214insTAAA | |
ENST00000464077.1:n.339+213_339+214insTAAA | ||
NM_017625.2:c.405+213_405+214insTAAA | NP_060095.2:n.405+213_405+214insTAAA | |
NM_017625.3:c.405+213_405+214insTAAA MANE Select | NP_060095.2:n.405+213_405+214insTAAA |