HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085862_186085863delinsGT , CM000666.2:g.186085862_186085863delinsGT | GRCh38 |
NC_000004.11:g.187007016_187007017delinsGT , CM000666.1:g.187007016_187007017delinsGT | GRCh37 |
NC_000004.10:g.187244010_187244011delinsGT | NCBI36 |
NG_007278.1:g.21708_21709delinsGT , LRG_117:g.21708_21709delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*3256_*3257delinsGT | ENSP00000513675.1:n.*3256_*3257delinsGT | |
ENST00000698353.1:n.3579_3580delinsGT | ||
ENST00000698354.1:c.*989_*990delinsGT | ENSP00000513676.1:n.*989_*990delinsGT | |
ENST00000296795.8:c.*989_*990delinsGT MANE Select | ENSP00000296795.3:n.*989_*990delinsGT | |
ENST00000296795.7:c.*989_*990delinsGT | ENSP00000296795.2:n.*989_*990delinsGT | |
NM_003265.3:c.*989_*990delinsGT MANE Select | NP_003256.1:n.*989_*990delinsGT |