HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24258225del , CM000676.2:g.24258225del | GRCh38 |
NC_000014.8:g.24727431del , CM000676.1:g.24727431del | GRCh37 |
NC_000014.7:g.23797271del | NCBI36 |
NG_007150.1:g.9942del | |
NG_007150.2:g.9942del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000206765.11:c.1402+60del MANE Select | ENSP00000206765.6:n.1402+60del | |
ENST00000206765.10:c.1402+60del | ENSP00000206765.6:n.1402+60del | |
ENST00000544573.5:c.76+60del | ENSP00000439446.1:n.76+60del | |
ENST00000559136.1:c.475+60del | ENSP00000453337.1:n.475+60del | |
NM_000359.2:c.1402+60del | NP_000350.1:n.1402+60del | |
NM_000359.3:c.1402+60del MANE Select | NP_000350.1:n.1402+60del |