HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19957744_19957746delinsAAG , CM000670.2:g.19957744_19957746delinsAAG | GRCh38 |
NC_000008.10:g.19815255_19815257delinsAAG , CM000670.1:g.19815255_19815257delinsAAG | GRCh37 |
NC_000008.9:g.19859535_19859537delinsAAG | NCBI36 |
NG_008855.1:g.23674_23676delinsAAG | |
NG_008855.2:g.61028_61030delinsAAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1019-1516_1019-1514delinsAAG MANE Select | ENSP00000497642.1:n.1019-1516_1019-1514de... | |
ENST00000650478.1:c.79+1661_79+1663delinsAAG | ENSP00000497560.1:n.79+1661_79+1663delins... | |
ENST00000311322.8:c.1019-1516_1019-1514delinsAAG | ENSP00000309757.6:n.1019-1516_1019-1514de... | |
NM_000237.2:c.1019-1516_1019-1514delinsAAG | NP_000228.1:n.1019-1516_1019-1514delinsAA... | |
NM_000237.3:c.1019-1516_1019-1514delinsAAG MANE Select | NP_000228.1:n.1019-1516_1019-1514delinsAA... |