HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2445390dup , CM000673.2:g.2445390dup | GRCh38 |
NC_000011.9:g.2466620dup , CM000673.1:g.2466620dup | GRCh37 |
NC_000011.8:g.2423196dup | NCBI36 |
NG_008935.1:g.5400dup , LRG_287:g.5400dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496887.7:c.31dup | ENSP00000434560.2:p.Arg11ProfsTer? | |
ENST00000646564.2:c.292dup | ENSP00000495806.2:p.Arg98ProfsTer? | |
ENST00000155840.12:c.292dup MANE Select | ENSP00000155840.2:p.Arg98ProfsTer? | |
ENST00000155840.9:c.292dup | ENSP00000155840.2:p.Arg98ProfsTer? | |
ENST00000345015.4:n.69dup | ||
ENST00000496887.6:c.31dup | ENSP00000434560.1:p.Arg11ProfsTer? | |
NM_000218.2:c.292dup , LRG_287t1:c.292dup | NP_000209.2:p.Arg98ProfsTer? | |
NM_000218.3:c.292dup MANE Select | NP_000209.2:p.Arg98ProfsTer? |