HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94030552_94030553insACTC , CM000663.2:g.94030552_94030553insACTC | GRCh38 |
NC_000001.10:g.94496108_94496109insACTC , CM000663.1:g.94496108_94496109insACTC | GRCh37 |
NC_000001.9:g.94268696_94268697insACTC | NCBI36 |
NG_009073.1:g.95597_95598insGAGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4254-27_4254-26insGAGT MANE Select | ENSP00000359245.3:n.4254-27_4254-26insGAGT | |
ENST00000370225.3:c.4254-27_4254-26insGAGT | ENSP00000359245.3:n.4254-27_4254-26insGAGT | |
ENST00000536513.5:c.630-27_630-26insGAGT | ENSP00000439707.2:n.630-27_630-26insGAGT | |
NM_000350.2:c.4254-27_4254-26insGAGT | NP_000341.2:n.4254-27_4254-26insGAGT | |
NM_000350.3:c.4254-27_4254-26insGAGT MANE Select | NP_000341.2:n.4254-27_4254-26insGAGT |