HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68430055_68430056insCTTGCTTTA , CM000663.2:g.68430055_68430056insCTTGCTTTA | GRCh38 |
NC_000001.10:g.68895738_68895739insCTTGCTTTA , CM000663.1:g.68895738_68895739insCTTGCTTTA | GRCh37 |
NC_000001.9:g.68668326_68668327insCTTGCTTTA | NCBI36 |
NG_008472.1:g.24904_24905insTAAAGCAAG | |
NG_008472.2:g.24904_24905insTAAAGCAAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.1451-129_1451-128insTAAAGCAAG MANE Select | ENSP00000262340.5:n.1451-129_1451-128insTAAAGCAAG | |
ENST00000262340.5:c.1451-129_1451-128insTAAAGCAAG | ENSP00000262340.5:n.1451-129_1451-128insTAAAGCAAG | |
NM_000329.2:c.1451-129_1451-128insTAAAGCAAG | NP_000320.1:n.1451-129_1451-128insTAAAGCAAG | |
XM_017002027.1:c.1175-129_1175-128insTAAAGCAAG | XP_016857516.1:n.1175-129_1175-128insTAAAGCAAG | |
NM_000329.3:c.1451-129_1451-128insTAAAGCAAG MANE Select | NP_000320.1:n.1451-129_1451-128insTAAAGCAAG |