HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085845_186085846delinsTG , CM000666.2:g.186085845_186085846delinsTG | GRCh38 |
NC_000004.11:g.187006999_187007000delinsTG , CM000666.1:g.187006999_187007000delinsTG | GRCh37 |
NC_000004.10:g.187243993_187243994delinsTG | NCBI36 |
NG_007278.1:g.21691_21692delinsTG , LRG_117:g.21691_21692delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3239_*3240delinsTG | ENSP00000513675.1:n.*3239_*3240delinsTG | |
ENST00000698353.1:n.3562_3563delinsTG | ||
ENST00000698354.1:c.*972_*973delinsTG | ENSP00000513676.1:n.*972_*973delinsTG | |
ENST00000296795.8:c.*972_*973delinsTG MANE Select | ENSP00000296795.3:n.*972_*973delinsTG | |
ENST00000296795.7:c.*972_*973delinsTG | ENSP00000296795.2:n.*972_*973delinsTG | |
NM_003265.3:c.*972_*973delinsTG MANE Select | NP_003256.1:n.*972_*973delinsTG |