HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215675673_215675674insA , CM000663.2:g.215675673_215675674insA | GRCh38 |
NC_000001.10:g.215849015_215849016insA , CM000663.1:g.215849015_215849016insA | GRCh37 |
NC_000001.9:g.213915638_213915639insA | NCBI36 |
NG_009497.1:g.752723_752724insT | |
NG_009497.2:g.752775_752776insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.12295-58_12295-57insT MANE Select | ENSP00000305941.3:n.12295-58_12295-57insT | |
ENST00000674083.1:c.12295-58_12295-57insT | ENSP00000501296.1:n.12295-58_12295-57insT | |
ENST00000307340.7:c.12295-58_12295-57insT | ENSP00000305941.3:n.12295-58_12295-57insT | |
NM_206933.2:c.12295-58_12295-57insT | NP_996816.2:n.12295-58_12295-57insT | |
NM_206933.3:c.12295-58_12295-57insT | NP_996816.2:n.12295-58_12295-57insT | |
NM_206933.4:c.12295-58_12295-57insT MANE Select | NP_996816.3:n.12295-58_12295-57insT |