HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734137_4734138delinsTG , CM000679.2:g.4734137_4734138delinsTG | GRCh38 |
NC_000017.10:g.4637432_4637433delinsTG , CM000679.1:g.4637432_4637433delinsTG | GRCh37 |
NC_000017.9:g.4584181_4584182delinsTG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*365_*366delinsCA MANE Select | ENSP00000293778.7:n.*365_*366delinsCA | |
ENST00000293778.10:c.*365_*366delinsCA | ENSP00000293778.6:n.*365_*366delinsCA | |
ENST00000576153.5:n.921_922delinsCA | ||
NM_022059.3:c.*365_*366delinsCA | NP_071342.2:n.*365_*366delinsCA | |
NM_022059.4:c.*365_*366delinsCA | NP_071342.2:n.*365_*366delinsCA | |
NM_001386809.1:c.*365_*366delinsCA MANE Select | NP_001373738.1:n.*365_*366delinsCA |