HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68646937_68646938insAAC , CM000666.2:g.68646937_68646938insAAC | GRCh38 |
NC_000004.11:g.69512655_69512656insAAC , CM000666.1:g.69512655_69512656insAAC | GRCh37 |
NC_000004.10:g.69195250_69195251insAAC | NCBI36 |
NG_052676.1:g.28840_28841insTTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.*167_*168insTTG MANE Select | ENSP00000341045.5:n.*167_*168insTTG | |
ENST00000338206.5:c.*167_*168insTTG | ENSP00000341045.5:n.*167_*168insTTG | |
ENST00000616841.4:c.1732+28_1732+29insTTG | ENSP00000482004.1:n.1732+28_1732+29insTTG | |
NM_001076.3:c.*167_*168insTTG | NP_001067.2:n.*167_*168insTTG | |
NM_001076.4:c.*167_*168insTTG MANE Select | NP_001067.2:n.*167_*168insTTG |