HGVS | Genome Assembly |
---|---|
NC_000019.10:g.45766941del , CM000681.2:g.45766941del | GRCh38 |
NC_000019.9:g.46270199del , CM000681.1:g.46270199del | GRCh37 |
NC_000019.8:g.50962039del | NCBI36 |
NG_012745.1:g.7303del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000317578.7:c.1022del MANE Select | ENSP00000316842.4:p.Gly341AlafsTer? | |
ENST00000317578.6:c.1022del | ENSP00000316842.4:p.Gly341AlafsTer? | |
ENST00000560160.1:c.587-826del | ||
ENST00000560168.1:c.*210del | ENSP00000453189.2:n.*210del | |
ENST00000622857.1:c.16-975del | ENSP00000481365.1:n.16-975del | |
NM_175875.4:c.1022del | NP_787071.2:p.Gly341AlafsTer? | |
NM_175875.5:c.1022del MANE Select | NP_787071.3:p.Gly341AlafsTer? |