HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48045714dup , CM000675.2:g.48045714dup | GRCh38 |
NC_000013.10:g.48619850dup , CM000675.1:g.48619850dup | GRCh37 |
NC_000013.9:g.47517851dup | NCBI36 |
NG_047021.1:g.13148dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258662.3:c.410dup MANE Select | ENSP00000258662.1:p.Leu138ThrfsTer10 | |
ENST00000258662.2:c.410dup | ENSP00000258662.1:p.Leu138ThrfsTer10 | |
NM_018283.2:c.410dup | NP_060753.1:p.Leu138ThrfsTer10 | |
NM_018283.3:c.410dup | NP_060753.1:p.Leu138ThrfsTer10 | |
NR_136687.1:n.590dup | ||
NR_136688.1:n.590dup | ||
NM_018283.4:c.410dup MANE Select | NP_060753.1:p.Leu138ThrfsTer10 | |
NR_136687.2:n.431dup | ||
NR_136688.2:n.431dup |