HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74752057_74752059delinsAAG , CM000677.2:g.74752057_74752059delinsAAG | GRCh38 |
NC_000015.9:g.75044398_75044400delinsAAG , CM000677.1:g.75044398_75044400delinsAAG | GRCh37 |
NC_000015.8:g.72831451_72831453delinsAAG | NCBI36 |
NG_008431.1:g.34516_34518delinsAAG | |
NG_008431.2:g.34516_34518delinsAAG | |
NG_061543.1:g.8213_8215delinsAAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000343932.5:c.1043-67_1043-65delinsAAG MANE Select | ENSP00000342007.4:n.1043-67_1043-65delins... | |
ENST00000343932.4:c.1043-67_1043-65delinsAAG | ENSP00000342007.4:n.1043-67_1043-65delins... | |
NM_000761.4:c.1043-67_1043-65delinsAAG | NP_000752.2:n.1043-67_1043-65delinsAAG | |
NM_000761.5:c.1043-67_1043-65delinsAAG MANE Select | NP_000752.2:n.1043-67_1043-65delinsAAG |