HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734282_4734285delinsATTT , CM000679.2:g.4734282_4734285delinsATTT | GRCh38 |
NC_000017.10:g.4637577_4637580delinsATTT , CM000679.1:g.4637577_4637580delinsATTT | GRCh37 |
NC_000017.9:g.4584326_4584329delinsATTT | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*218_*221delinsAAAT MANE Select | ENSP00000293778.7:n.*218_*221delinsAAAT | |
ENST00000293778.10:c.*218_*221delinsAAAT | ENSP00000293778.6:n.*218_*221delinsAAAT | |
ENST00000576153.5:n.774_777delinsAAAT | ||
NM_022059.3:c.*218_*221delinsAAAT | NP_071342.2:n.*218_*221delinsAAAT | |
NM_022059.4:c.*218_*221delinsAAAT | NP_071342.2:n.*218_*221delinsAAAT | |
NM_001386809.1:c.*218_*221delinsAAAT MANE Select | NP_001373738.1:n.*218_*221delinsAAAT |