HGVS | Genome Assembly |
---|---|
NC_000019.10:g.3926019_3926020insT , CM000681.2:g.3926019_3926020insT | GRCh38 |
NC_000019.9:g.3926017_3926018insT , CM000681.1:g.3926017_3926018insT | GRCh37 |
NC_000019.8:g.3877017_3877018insT | NCBI36 |
NG_012638.1:g.50400_50401insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450849.7:c.*1427_*1428insT MANE Select | ENSP00000390941.1:n.*1427_*1428insT | |
ENST00000450849.6:c.*1427_*1428insT | ENSP00000390941.1:n.*1427_*1428insT | |
ENST00000600960.1:c.2607_2608insT | ENSP00000470842.1:n.2607_2608insT | |
ENST00000601323.1:n.440-239_440-238insT | ||
NM_033064.4:c.*1427_*1428insT | NP_149053.1:n.*1427_*1428insT | |
NM_033064.5:c.*1427_*1428insT MANE Select | NP_149053.1:n.*1427_*1428insT |