HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734219_4734224delinsGCAAAA , CM000679.2:g.4734219_4734224delinsGCAAAA | GRCh38 |
NC_000017.10:g.4637514_4637519delinsGCAAAA , CM000679.1:g.4637514_4637519delinsGCAAAA | GRCh37 |
NC_000017.9:g.4584263_4584268delinsGCAAAA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*279_*284delinsTTTTGC MANE Select | ENSP00000293778.7:n.*279_*284delinsTTTTGC | |
ENST00000293778.10:c.*279_*284delinsTTTTGC | ENSP00000293778.6:n.*279_*284delinsTTTTGC | |
ENST00000576153.5:n.835_840delinsTTTTGC | ||
NM_022059.3:c.*279_*284delinsTTTTGC | NP_071342.2:n.*279_*284delinsTTTTGC | |
NM_022059.4:c.*279_*284delinsTTTTGC | NP_071342.2:n.*279_*284delinsTTTTGC | |
NM_001386809.1:c.*279_*284delinsTTTTGC MANE Select | NP_001373738.1:n.*279_*284delinsTTTTGC |