HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31719237_31719240dup , CM000668.2:g.31719237_31719240dup | GRCh38 |
NC_000006.11:g.31687014_31687017dup , CM000668.1:g.31687014_31687017dup | GRCh37 |
NC_000006.10:g.31794993_31794996dup | NCBI36 |
NG_029044.1:g.894_897dup | |
NG_029044.2:g.894_897dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375819.3:c.238_241dup (LY6G6C) MANE Select | ENSP00000364978.2:p.Arg81GlnfsTer9 | |
ENST00000375819.2:c.238_241dup (LY6G6C) | ENSP00000364978.2:p.Arg81GlnfsTer9 | |
ENST00000460663.5:n.90+554_90+557dup (MPIG6B) | ||
ENST00000495859.1:c.70_73dup (LY6G6C) | ENSP00000433207.1:p.Arg25GlnfsTer9 | |
NM_025261.2:c.238_241dup (LY6G6C) | NP_079537.1:p.Arg81GlnfsTer9 | |
NM_025261.3:c.238_241dup (LY6G6C) MANE Select | NP_079537.1:p.Arg81GlnfsTer9 |