HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085485_186085486delinsTG , CM000666.2:g.186085485_186085486delinsTG | GRCh38 |
NC_000004.11:g.187006639_187006640delinsTG , CM000666.1:g.187006639_187006640delinsTG | GRCh37 |
NC_000004.10:g.187243633_187243634delinsTG | NCBI36 |
NG_007278.1:g.21331_21332delinsTG , LRG_117:g.21331_21332delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*2879_*2880delinsTG | ENSP00000513675.1:n.*2879_*2880delinsTG | |
ENST00000698353.1:n.3202_3203delinsTG | ||
ENST00000698354.1:c.*612_*613delinsTG | ENSP00000513676.1:n.*612_*613delinsTG | |
ENST00000296795.8:c.*612_*613delinsTG MANE Select | ENSP00000296795.3:n.*612_*613delinsTG | |
ENST00000296795.7:c.*612_*613delinsTG | ENSP00000296795.2:n.*612_*613delinsTG | |
NM_003265.3:c.*612_*613delinsTG MANE Select | NP_003256.1:n.*612_*613delinsTG |