HGVS | Genome Assembly |
---|---|
NC_000005.10:g.111071929_111071932del , CM000667.2:g.111071929_111071932del | GRCh38 |
NC_000005.9:g.110407627_110407630del , CM000667.1:g.110407627_110407630del | GRCh37 |
NC_000005.8:g.110435526_110435529del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000344895.4:c.39_42del MANE Select | ENSP00000339804.3:p.Phe14GlyfsTer9 | |
ENST00000344895.3:c.39_42del | ENSP00000339804.3:p.Phe14GlyfsTer9 | |
ENST00000420978.6:c.39_42del | ENSP00000399099.2:p.Phe14GlyfsTer9 | |
NM_033035.4:c.39_42del | NP_149024.1:p.Phe14GlyfsTer9 | |
NR_045089.1:n.1443_1446del | ||
NM_033035.5:c.39_42del MANE Select | NP_149024.1:p.Phe14GlyfsTer9 | |
NR_045089.2:n.1461_1464del |