HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94008289_94008290delinsCA , CM000663.2:g.94008289_94008290delinsCA | GRCh38 |
NC_000001.10:g.94473845_94473846delinsCA , CM000663.1:g.94473845_94473846delinsCA | GRCh37 |
NC_000001.9:g.94246433_94246434delinsCA | NCBI36 |
NG_009073.1:g.117860_117861delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.5843_5844delinsTG MANE Select | ENSP00000359245.3:p.Pro1948Leu | |
ENST00000370225.3:c.5843_5844delinsTG | ENSP00000359245.3:p.Pro1948Leu | |
ENST00000465352.1:n.259_260delinsTG | ||
ENST00000536513.5:c.2219_2220delinsTG | ENSP00000439707.2:p.Pro740Leu | |
NM_000350.2:c.5843_5844delinsTG | NP_000341.2:p.Pro1948Leu | |
NM_000350.3:c.5843_5844delinsTG MANE Select | NP_000341.2:p.Pro1948Leu |