HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94021731_94021733delinsCAA , CM000663.2:g.94021731_94021733delinsCAA | GRCh38 |
NC_000001.10:g.94487287_94487289delinsCAA , CM000663.1:g.94487287_94487289delinsCAA | GRCh37 |
NC_000001.9:g.94259875_94259877delinsCAA | NCBI36 |
NG_009073.1:g.104417_104419delinsTTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4774-19_4774-17delinsTTG MANE Select | ENSP00000359245.3:n.4774-19_4774-17delinsTTG | |
ENST00000370225.3:c.4774-19_4774-17delinsTTG | ENSP00000359245.3:n.4774-19_4774-17delinsTTG | |
ENST00000460514.1:n.268-19_268-17delinsTTG | ||
ENST00000536513.5:c.1150-19_1150-17delinsTTG | ENSP00000439707.2:n.1150-19_1150-17delinsTTG | |
NM_000350.2:c.4774-19_4774-17delinsTTG | NP_000341.2:n.4774-19_4774-17delinsTTG | |
NM_000350.3:c.4774-19_4774-17delinsTTG MANE Select | NP_000341.2:n.4774-19_4774-17delinsTTG |