HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94043391_94043392insT , CM000663.2:g.94043391_94043392insT | GRCh38 |
NC_000001.10:g.94508947_94508948insT , CM000663.1:g.94508947_94508948insT | GRCh37 |
NC_000001.9:g.94281535_94281536insT | NCBI36 |
NG_009073.1:g.82758_82759insA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.3134_3135insA MANE Select | ENSP00000359245.3:p.Met1045IlefsTer13 | |
ENST00000370225.3:c.3134_3135insA | ENSP00000359245.3:p.Met1045IlefsTer13 | |
ENST00000536513.5:c.-64-3303_-64-3302insA | ENSP00000439707.2:n.-64-3303_-64-3302insA... | |
NM_000350.2:c.3134_3135insA | NP_000341.2:p.Met1045IlefsTer13 | |
NM_000350.3:c.3134_3135insA MANE Select | NP_000341.2:p.Met1045IlefsTer13 |