HGVS | Genome Assembly |
---|---|
NC_000023.11:g.116172578_116172579delinsTG , CM000685.2:g.116172578_116172579delinsTG | GRCh38 |
NC_000023.10:g.115303831_115303832delinsTG , CM000685.1:g.115303831_115303832delinsTG | GRCh37 |
NC_000023.9:g.115217859_115217860delinsTG | NCBI36 |
NG_016326.1:g.6874_6875delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371906.5:c.298_299delinsTG MANE Select | ENSP00000360973.4:p.Trp100= | |
ENST00000680409.1:n.766_767delinsTG | ||
ENST00000681852.1:c.298_299delinsTG | ENSP00000505750.1:p.Trp100= | |
ENST00000371906.4:c.298_299delinsTG | ENSP00000360973.4:p.Trp100= | |
NM_000686.4:c.298_299delinsTG | NP_000677.2:p.Trp100= | |
XM_011537533.1:c.298_299delinsTG | XP_011535835.1:p.Trp100= | |
NM_000686.5:c.298_299delinsTG MANE Select | NP_000677.2:p.Trp100= | |
NM_001385624.1:c.298_299delinsTG | NP_001372553.1:p.Trp100= |