HGVS | Genome Assembly |
---|---|
NC_000020.11:g.6770386_6770387insG , CM000682.2:g.6770386_6770387insG | GRCh38 |
NC_000020.10:g.6751033_6751034insG , CM000682.1:g.6751033_6751034insG | GRCh37 |
NC_000020.9:g.6699033_6699034insG | NCBI36 |
NG_023233.1:g.7289_7290insG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000378827.5:c.260_261insG MANE Select | ENSP00000368104.3:p.Gly88ArgfsTer28 | |
ENST00000378827.4:c.260_261insG | ENSP00000368104.3:p.Gly88ArgfsTer28 | |
NM_001200.2:c.260_261insG | NP_001191.1:p.Gly88ArgfsTer28 | |
XM_011529323.1:c.-123+1511_-123+1512insG | XP_011527625.1:n.-123+1511_-123+1512insG | |
NM_001200.3:c.260_261insG | NP_001191.1:p.Gly88ArgfsTer28 | |
NM_001200.4:c.260_261insG MANE Select | NP_001191.1:p.Gly88ArgfsTer28 |