HGVS | Genome Assembly |
---|---|
NC_000015.10:g.38356500_38356503delinsTAAG , CM000677.2:g.38356500_38356503delinsTAAG | GRCh38 |
NC_000015.9:g.38648701_38648704delinsTAAG , CM000677.1:g.38648701_38648704delinsTAAG | GRCh37 |
NC_000015.8:g.36435993_36435996delinsTAAG | NCBI36 |
NG_008980.1:g.108650_108653delinsTAAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000299084.9:c.*4836_*4839delinsTAAG MANE Select | ENSP00000299084.4:n.*4836_*4839delinsTAAG... | |
ENST00000299084.8:c.*4836_*4839delinsTAAG | ENSP00000299084.4:n.*4836_*4839delinsTAAG... | |
NM_152594.2:c.*4836_*4839delinsTAAG | NP_689807.1:n.*4836_*4839delinsTAAG | |
XM_005254202.3:c.*4836_*4839delinsTAAG | XP_005254259.1:n.*4836_*4839delinsTAAG | |
XM_011521289.3:c.*4836_*4839delinsTAAG | XP_011519591.1:n.*4836_*4839delinsTAAG | |
NM_152594.3:c.*4836_*4839delinsTAAG MANE Select | NP_689807.1:n.*4836_*4839delinsTAAG |