HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215867171_215867173delinsTT , CM000663.2:g.215867171_215867173delinsTT | GRCh38 |
NC_000001.10:g.216040513_216040515delinsTT , CM000663.1:g.216040513_216040515delinsTT | GRCh37 |
NC_000001.9:g.214107136_214107138delinsTT | NCBI36 |
NG_009497.1:g.561224_561226delinsAA | |
NG_009497.2:g.561276_561278delinsAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.8682-3_8682-1delinsAA MANE Select | ENSP00000305941.3:n.8682-3_8682-1delinsAA | |
ENST00000674083.1:c.8682-3_8682-1delinsAA | ENSP00000501296.1:n.8682-3_8682-1delinsAA | |
ENST00000307340.7:c.8682-3_8682-1delinsAA | ENSP00000305941.3:n.8682-3_8682-1delinsAA | |
NM_206933.2:c.8682-3_8682-1delinsAA | NP_996816.2:n.8682-3_8682-1delinsAA | |
NM_206933.3:c.8682-3_8682-1delinsAA | NP_996816.2:n.8682-3_8682-1delinsAA | |
NM_206933.4:c.8682-3_8682-1delinsAA MANE Select | NP_996816.3:n.8682-3_8682-1delinsAA |