HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085844_186085846delinsTTG , CM000666.2:g.186085844_186085846delinsTTG | GRCh38 |
NC_000004.11:g.187006998_187007000delinsTTG , CM000666.1:g.187006998_187007000delinsTTG | GRCh37 |
NC_000004.10:g.187243992_187243994delinsTTG | NCBI36 |
NG_007278.1:g.21690_21692delinsTTG , LRG_117:g.21690_21692delinsTTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3238_*3240delinsTTG | ENSP00000513675.1:n.*3238_*3240delinsTTG | |
ENST00000698353.1:n.3561_3563delinsTTG | ||
ENST00000698354.1:c.*971_*973delinsTTG | ENSP00000513676.1:n.*971_*973delinsTTG | |
ENST00000296795.8:c.*971_*973delinsTTG MANE Select | ENSP00000296795.3:n.*971_*973delinsTTG | |
ENST00000296795.7:c.*971_*973delinsTTG | ENSP00000296795.2:n.*971_*973delinsTTG | |
NM_003265.3:c.*971_*973delinsTTG MANE Select | NP_003256.1:n.*971_*973delinsTTG |