HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70177197_70177205delinsCTCACCGAG , CM000679.2:g.70177197_70177205delinsCTCACCGAG | GRCh38 |
NC_000017.10:g.68173338_68173346delinsCTCACCGAG , CM000679.1:g.68173338_68173346delinsCTCACCGAG | GRCh37 |
NC_000017.9:g.65684933_65684941delinsCTCACCGAG | NCBI36 |
NG_008798.1:g.12663_12671delinsCTCACCGAG , LRG_328:g.12663_12671delinsCTCACCGAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000243457.4:c.*874_*882delinsCTCACCGAG MANE Select | ENSP00000243457.2:n.*874_*882delinsCTCACC... | |
ENST00000243457.3:c.*874_*882delinsCTCACCGAG | ENSP00000243457.2:n.*874_*882delinsCTCACC... | |
NM_000891.2:c.*874_*882delinsCTCACCGAG , LRG_328t1:c.*874_*882delinsCTCACCGAG | NP_000882.1:n.*874_*882delinsCTCACCGAG | |
XM_011524779.1:c.*874_*882delinsCTCACCGAG | XP_011523081.1:n.*874_*882delinsCTCACCGAG... | |
NM_000891.3:c.*874_*882delinsCTCACCGAG MANE Select | NP_000882.1:n.*874_*882delinsCTCACCGAG |