HGVS | Genome Assembly |
---|---|
NC_000001.11:g.206116602_206116603insTCCAGCGGTAGGT , CM000663.2:g.206116602_206116603insTCCAGCGGTAGGT | GRCh38 |
NC_000001.10:g.206224738_206224739insGGAACCTACCGCT , CM000663.1:g.206224738_206224739insGGAACCTACCGCT | GRCh37 |
NC_000001.9:g.204391361_204391362insGGAACCTACCGCT | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000367126.5:c.298_299insGGAACCTACCGCT MANE Select | ENSP00000356094.4:p.Phe100TrpfsTer? | |
ENST00000367126.4:c.298_299insGGAACCTACCGCT | ENSP00000356094.4:p.Phe100TrpfsTer? | |
ENST00000612906.1:n.36+1071_36+1072insGGAACCTACCGCT | ||
NM_000707.3:c.298_299insGGAACCTACCGCT | NP_000698.1:p.Phe100TrpfsTer? | |
NM_000707.4:c.298_299insGGAACCTACCGCT | NP_000698.1:p.Phe100TrpfsTer? | |
NM_000707.5:c.298_299insGGAACCTACCGCT MANE Select | NP_000698.1:p.Phe100TrpfsTer? |