HGVS | Genome Assembly |
---|---|
NC_000011.10:g.67586536dup , CM000673.2:g.67586536dup | GRCh38 |
NC_000011.9:g.67354007dup , CM000673.1:g.67354007dup | GRCh37 |
NC_000011.8:g.67110583dup | NCBI36 |
NG_012075.1:g.7942dup , LRG_723:g.7942dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000398603.6:c.484dup | ENSP00000381604.1:p.Glu162GlyfsTer? | |
ENST00000398606.10:c.592dup MANE Select | ENSP00000381607.3:p.Glu198GlyfsTer? | |
ENST00000398603.5:c.484dup | ENSP00000381604.1:p.Glu162GlyfsTer? | |
ENST00000398606.7:c.592dup | ENSP00000381607.3:p.Glu198GlyfsTer? | |
ENST00000467591.1:n.703dup | ||
ENST00000494593.1:n.1564dup | ||
ENST00000498765.5:c.655dup | ||
NM_000852.3:c.592dup , LRG_723t1:c.592dup | NP_000843.1:p.Glu198GlyfsTer? | |
NM_000852.4:c.592dup MANE Select | NP_000843.1:p.Glu198GlyfsTer? |