HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23418343_23418344delinsTT , CM000676.2:g.23418343_23418344delinsTT | GRCh38 |
NC_000014.8:g.23887552_23887553delinsTT , CM000676.1:g.23887552_23887553delinsTT | GRCh37 |
NC_000014.7:g.22957392_22957393delinsTT | NCBI36 |
NG_007884.1:g.22318_22319delinsAA , LRG_384:g.22318_22319delinsAA |
HGVS | Amino-acid Change |
---|---|
NM_000257.4:c.4035_4036delinsAA MANE Select | NP_000248.2:p.Gln1346Lys |
ENST00000355349.4:c.4035_4036delinsAA MANE Select | ENSP00000347507.3:p.Gln1346Lys |
NM_000257.3:c.4035_4036delinsAA | NP_000248.2:p.Gln1346Lys |
ENST00000355349.3:c.4035_4036delinsAA | ENSP00000347507.3:p.Gln1346Lys |
XM_017021340.1:c.4035_4036delinsAA | XP_016876829.1:p.Gln1346Lys |