HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713857_114713883dup , CM000663.2:g.114713857_114713883dup | GRCh38 |
NC_000001.10:g.115256478_115256504dup , CM000663.1:g.115256478_115256504dup | GRCh37 |
NC_000001.9:g.115058001_115058027dup | NCBI36 |
NG_007572.1:g.8014_8040dup , LRG_92:g.8014_8040dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.209_235dup MANE Select | ENSP00000358548.4:p.Phe78_Leu79insGlnTyrMetArgThrGlyGluGlyPhe... | |
ENST00000369535.4:c.209_235dup | ENSP00000358548.4:p.Phe78_Leu79insGlnTyrMetArgThrGlyGluGlyPhe... | |
NM_002524.4:c.209_235dup | NP_002515.1:p.Phe78_Leu79insGlnTyrMetArgThrGlyGluGlyPhe | |
NM_002524.5:c.209_235dup MANE Select | NP_002515.1:p.Phe78_Leu79insGlnTyrMetArgThrGlyGluGlyPhe |