HGVS | Genome Assembly |
---|---|
NC_000021.9:g.41756653_41756654delinsTT , CM000683.2:g.41756653_41756654delinsTT | GRCh38 |
NC_000021.8:g.43176813_43176814delinsTT , CM000683.1:g.43176813_43176814delinsTT | GRCh37 |
NC_000021.7:g.42049882_42049883delinsTT | NCBI36 |
NG_032113.1:g.15436_15437delinsAA | |
NG_032113.2:g.15436_15437delinsAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000332512.8:c.345_346delinsAA MANE Select | ENSP00000332454.3:p.Trp115Ter | |
ENST00000332512.7:c.345_346delinsAA | ENSP00000332454.3:p.Trp115Ter | |
ENST00000352483.3:c.345_346delinsAA | ENSP00000330161.2:p.Trp115Ter | |
NM_020639.2:c.345_346delinsAA | NP_065690.2:p.Trp115Ter | |
NM_020639.3:c.345_346delinsAA MANE Select | NP_065690.2:p.Trp115Ter |