HGVS | Genome Assembly |
---|---|
NC_000001.11:g.193251997_193251998insCT , CM000663.2:g.193251997_193251998insCT | GRCh38 |
NC_000001.10:g.193221127_193221128insCT , CM000663.1:g.193221127_193221128insCT | GRCh37 |
NC_000001.9:g.191487750_191487751insCT | NCBI36 |
NG_012691.1:g.135040_135041insCT , LRG_507:g.135040_135041insCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367435.5:c.*1285_*1286insCT MANE Select | ENSP00000356405.4:n.*1285_*1286insCT | |
ENST00000635846.1:c.*1285_*1286insCT | ENSP00000490035.1:n.*1285_*1286insCT | |
ENST00000643006.1:c.*1791_*1792insCT | ENSP00000496633.1:n.*1791_*1792insCT | |
ENST00000367435.3:c.*1285_*1286insCT | ENSP00000356405.3:n.*1285_*1286insCT | |
NM_024529.4:c.*1285_*1286insCT , LRG_507t1:c.*1285_*1286insCT | NP_078805.3:n.*1285_*1286insCT | |
NM_024529.5:c.*1285_*1286insCT MANE Select | NP_078805.3:n.*1285_*1286insCT |