HGVS | Genome Assembly |
---|---|
NC_000007.14:g.107717393_107717421delinsGTGAATGTAATAGTCTTGCAGAAAATGAA , CM000669.2:g.107717393_107717421delinsGTGAATGTAATAGTCTTGCAGAAAATGAA | GRCh38 |
NC_000007.13:g.107357838_107357866delinsGTGAATGTAATAGTCTTGCAGAAAATGAA , CM000669.1:g.107357838_107357866delinsGTGAATGTAATAGTCTTGCAGAAAATGAA | GRCh37 |
NC_000007.12:g.107145074_107145102delinsGTGAATGTAATAGTCTTGCAGAAAATGAA | NCBI36 |
NG_008489.1:g.61759_61787delinsGTGAATGTAATAGTCTTGCAGAAAATGAA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000644269.2:c.*1947_*1975delinsGTGAATGTAATAGTCTTGCAGAAAATGAA MANE Select | ENSP00000494017.1:n.*1947_*1975delinsGTGA... | |
ENST00000265715.7:c.*1947_*1975delinsGTGAATGTAATAGTCTTGCAGAAAATGAA | ENSP00000265715.3:n.*1947_*1975delinsGTGA... | |
NM_000441.1:c.*1947_*1975delinsGTGAATGTAATAGTCTTGCAGAAAATGAA | NP_000432.1:n.*1947_*1975delinsGTGAATGTAA... | |
NM_000441.2:c.*1947_*1975delinsGTGAATGTAATAGTCTTGCAGAAAATGAA MANE Select | NP_000432.1:n.*1947_*1975delinsGTGAATGTAA... |