HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4631145_4631146insGC , CM000679.2:g.4631145_4631146insGC | GRCh38 |
NC_000017.10:g.4534440_4534441insGC , CM000679.1:g.4534440_4534441insGC | GRCh37 |
NC_000017.9:g.4481189_4481190insGC | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293761.8:c.*454_*455insGC MANE Select | ENSP00000293761.3:n.*454_*455insGC | |
ENST00000293761.7:c.*454_*455insGC | ENSP00000293761.3:n.*454_*455insGC | |
ENST00000570836.5:c.*454_*455insGC | ENSP00000458832.1:n.*454_*455insGC | |
NM_001140.3:c.*454_*455insGC | NP_001131.3:n.*454_*455insGC | |
NM_001140.4:c.*454_*455insGC | NP_001131.3:n.*454_*455insGC | |
NM_001140.5:c.*454_*455insGC MANE Select | NP_001131.3:n.*454_*455insGC |