HGVS | Genome Assembly |
---|---|
NC_000002.12:g.27084919_27084922delinsTCAG , CM000664.2:g.27084919_27084922delinsTCAG | GRCh38 |
NC_000002.11:g.27307787_27307790delinsTCAG , CM000664.1:g.27307787_27307790delinsTCAG | GRCh37 |
NC_000002.10:g.27161291_27161294delinsTCAG | NCBI36 |
NG_012199.1:g.3177_3180delinsTCAG | |
NG_046849.1:g.11353_11356delinsTCAG | |
NG_012199.2:g.3177_3180delinsTCAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000380320.9:c.2558-72_2558-69delinsTCAG MANE Select | ENSP00000369677.4:n.2558-72_2558-69delins... | |
ENST00000380320.8:c.2558-72_2558-69delinsTCAG | ENSP00000369677.4:n.2558-72_2558-69delins... | |
ENST00000433140.1:c.550-72_550-69delinsTCAG | ||
NM_007046.3:c.2558-72_2558-69delinsTCAG | NP_008977.1:n.2558-72_2558-69delinsTCAG | |
XM_006711928.2:c.2558-72_2558-69delinsTCAG | XP_006711991.1:n.2558-72_2558-69delinsTCA... | |
NM_007046.4:c.2558-72_2558-69delinsTCAG MANE Select | NP_008977.1:n.2558-72_2558-69delinsTCAG |