HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734032_4734033delinsAC , CM000679.2:g.4734032_4734033delinsAC | GRCh38 |
NC_000017.10:g.4637327_4637328delinsAC , CM000679.1:g.4637327_4637328delinsAC | GRCh37 |
NC_000017.9:g.4584076_4584077delinsAC | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*470_*471delinsGT MANE Select | ENSP00000293778.7:n.*470_*471delinsGT | |
ENST00000293778.10:c.*470_*471delinsGT | ENSP00000293778.6:n.*470_*471delinsGT | |
ENST00000576153.5:n.1026_1027delinsGT | ||
NM_022059.3:c.*470_*471delinsGT | NP_071342.2:n.*470_*471delinsGT | |
NM_022059.4:c.*470_*471delinsGT | NP_071342.2:n.*470_*471delinsGT | |
NM_001386809.1:c.*470_*471delinsGT MANE Select | NP_001373738.1:n.*470_*471delinsGT |