HGVS | Genome Assembly |
---|---|
NC_000004.12:g.119320758_119320762delinsTTGAC , CM000666.2:g.119320758_119320762delinsTTGAC | GRCh38 |
NC_000004.11:g.120241913_120241917delinsTTGAC , CM000666.1:g.120241913_120241917delinsTTGAC | GRCh37 |
NC_000004.10:g.120461361_120461365delinsTTGAC | NCBI36 |
NG_011444.1:g.6400_6404delinsGTCAA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000274024.4:c.148_152delinsGTCAA MANE Select | ENSP00000274024.3:p.Val50= | |
ENST00000274024.3:c.148_152delinsGTCAA | ENSP00000274024.3:p.Val50= | |
NM_000134.3:c.148_152delinsGTCAA | NP_000125.2:p.Val50= | |
NM_000134.4:c.148_152delinsGTCAA MANE Select | NP_000125.2:p.Val50= |