HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734037_4734039delinsGTC , CM000679.2:g.4734037_4734039delinsGTC | GRCh38 |
NC_000017.10:g.4637332_4637334delinsGTC , CM000679.1:g.4637332_4637334delinsGTC | GRCh37 |
NC_000017.9:g.4584081_4584083delinsGTC | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*464_*466delinsGAC MANE Select | ENSP00000293778.7:n.*464_*466delinsGAC | |
ENST00000293778.10:c.*464_*466delinsGAC | ENSP00000293778.6:n.*464_*466delinsGAC | |
ENST00000576153.5:n.1020_1022delinsGAC | ||
NM_022059.3:c.*464_*466delinsGAC | NP_071342.2:n.*464_*466delinsGAC | |
NM_022059.4:c.*464_*466delinsGAC | NP_071342.2:n.*464_*466delinsGAC | |
NM_001386809.1:c.*464_*466delinsGAC MANE Select | NP_001373738.1:n.*464_*466delinsGAC |