HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4631195_4631196insGATGA , CM000679.2:g.4631195_4631196insGATGA | GRCh38 |
NC_000017.10:g.4534490_4534491insGATGA , CM000679.1:g.4534490_4534491insGATGA | GRCh37 |
NC_000017.9:g.4481239_4481240insGATGA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293761.8:c.*404_*405insTCATC MANE Select | ENSP00000293761.3:n.*404_*405insTCATC | |
ENST00000293761.7:c.*404_*405insTCATC | ENSP00000293761.3:n.*404_*405insTCATC | |
ENST00000570836.5:c.*404_*405insTCATC | ENSP00000458832.1:n.*404_*405insTCATC | |
NM_001140.3:c.*404_*405insTCATC | NP_001131.3:n.*404_*405insTCATC | |
NM_001140.4:c.*404_*405insTCATC | NP_001131.3:n.*404_*405insTCATC | |
NM_001140.5:c.*404_*405insTCATC MANE Select | NP_001131.3:n.*404_*405insTCATC |