HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734035_4734036insA , CM000679.2:g.4734035_4734036insA | GRCh38 |
NC_000017.10:g.4637330_4637331insA , CM000679.1:g.4637330_4637331insA | GRCh37 |
NC_000017.9:g.4584079_4584080insA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*467_*468insT MANE Select | ENSP00000293778.7:n.*467_*468insT | |
ENST00000293778.10:c.*467_*468insT | ENSP00000293778.6:n.*467_*468insT | |
ENST00000576153.5:n.1023_1024insT | ||
NM_022059.3:c.*467_*468insT | NP_071342.2:n.*467_*468insT | |
NM_022059.4:c.*467_*468insT | NP_071342.2:n.*467_*468insT | |
NM_001386809.1:c.*467_*468insT MANE Select | NP_001373738.1:n.*467_*468insT |