HGVS | Genome Assembly |
---|---|
NC_000014.9:g.28767665_28767676dup , CM000676.2:g.28767665_28767676dup | GRCh38 |
NC_000014.8:g.29236871_29236882dup , CM000676.1:g.29236871_29236882dup | GRCh37 |
NC_000014.7:g.28306622_28306633dup | NCBI36 |
NG_009367.1:g.5585_5596dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706482.1:c.386_397dup | ENSP00000516406.1:p.Gly132_Gly133insGluProGlyGly | |
ENST00000313071.7:c.386_397dup MANE Select | ENSP00000339004.3:p.Gly132_Gly133insGluProGlyGly | |
ENST00000313071.6:c.386_397dup | ENSP00000339004.3:p.Gly132_Gly133insGluProGlyGly | |
NM_005249.4:c.386_397dup | NP_005240.3:p.Gly132_Gly133insGluProGlyGly | |
NM_005249.5:c.386_397dup MANE Select | NP_005240.3:p.Gly132_Gly133insGluProGlyGly |