HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124873052_124873053insCT , CM000673.2:g.124873052_124873053insCT | GRCh38 |
NC_000011.9:g.124742948_124742949insCT , CM000673.1:g.124742948_124742949insCT | GRCh37 |
NC_000011.8:g.124248158_124248159insCT | NCBI36 |
NG_016214.1:g.12644_12645insCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397801.6:c.1499_1500insCT MANE Select | ENSP00000380903.1:p.Met501Ter | |
ENST00000397801.5:c.1499_1500insCT | ENSP00000380903.1:p.Met501Ter | |
ENST00000538940.5:c.1433_1434insCT | ENSP00000441797.1:p.Met479Ter | |
NM_022370.3:c.1499_1500insCT | NP_071765.2:p.Met501Ter | |
XM_011542953.1:c.2471_2472insCT | XP_011541255.1:p.Met825Ter | |
XM_017018122.1:c.1433_1434insCT | XP_016873611.1:p.Met479Ter | |
NM_022370.4:c.1499_1500insCT MANE Select | NP_071765.2:p.Met501Ter |