HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68646937_68646938insCAA , CM000666.2:g.68646937_68646938insCAA | GRCh38 |
NC_000004.11:g.69512655_69512656insCAA , CM000666.1:g.69512655_69512656insCAA | GRCh37 |
NC_000004.10:g.69195250_69195251insCAA | NCBI36 |
NG_052676.1:g.28839_28840insTTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.*166_*167insTTG MANE Select | ENSP00000341045.5:n.*166_*167insTTG | |
ENST00000338206.5:c.*166_*167insTTG | ENSP00000341045.5:n.*166_*167insTTG | |
ENST00000616841.4:c.1732+27_1732+28insTTG | ENSP00000482004.1:n.1732+27_1732+28insTTG | |
NM_001076.3:c.*166_*167insTTG | NP_001067.2:n.*166_*167insTTG | |
NM_001076.4:c.*166_*167insTTG MANE Select | NP_001067.2:n.*166_*167insTTG |