HGVS | Genome Assembly |
---|---|
NC_000008.11:g.37966151_37966157delinsCGCCCAA , CM000670.2:g.37966151_37966157delinsCGCCCAA | GRCh38 |
NC_000008.10:g.37823669_37823675delinsCGCCCAA , CM000670.1:g.37823669_37823675delinsCGCCCAA | GRCh37 |
NC_000008.9:g.37942826_37942832delinsCGCCCAA | NCBI36 |
NG_011936.1:g.5510_5516delinsTTGGGCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000345060.5:c.313_319delinsTTGGGCG MANE Select | ENSP00000343782.3:p.Leu105= | |
ENST00000520341.2:n.441_447delinsTTGGGCG | ||
ENST00000345060.4:c.313_319delinsTTGGGCG | ENSP00000343782.3:p.Leu105= | |
ENST00000614635.1:c.313_319delinsTTGGGCG | ENSP00000480325.1:p.Leu105= | |
NM_000025.2:c.313_319delinsTTGGGCG | NP_000016.1:p.Leu105= | |
NM_000025.3:c.313_319delinsTTGGGCG MANE Select | NP_000016.1:p.Leu105= |