HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085842_186085846delinsTTTTG , CM000666.2:g.186085842_186085846delinsTTTTG | GRCh38 |
NC_000004.11:g.187006996_187007000delinsTTTTG , CM000666.1:g.187006996_187007000delinsTTTTG | GRCh37 |
NC_000004.10:g.187243990_187243994delinsTTTTG | NCBI36 |
NG_007278.1:g.21688_21692delinsTTTTG , LRG_117:g.21688_21692delinsTTTTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3236_*3240delinsTTTTG | ENSP00000513675.1:n.*3236_*3240delinsTTTTG | |
ENST00000698353.1:n.3559_3563delinsTTTTG | ||
ENST00000698354.1:c.*969_*973delinsTTTTG | ENSP00000513676.1:n.*969_*973delinsTTTTG | |
ENST00000296795.8:c.*969_*973delinsTTTTG MANE Select | ENSP00000296795.3:n.*969_*973delinsTTTTG | |
ENST00000296795.7:c.*969_*973delinsTTTTG | ENSP00000296795.2:n.*969_*973delinsTTTTG | |
NM_003265.3:c.*969_*973delinsTTTTG MANE Select | NP_003256.1:n.*969_*973delinsTTTTG |