HGVS | Genome Assembly |
---|---|
NC_000023.11:g.25013245_25013268dup , CM000685.2:g.25013245_25013268dup | GRCh38 |
NC_000023.10:g.25031362_25031385dup , CM000685.1:g.25031362_25031385dup | GRCh37 |
NC_000023.9:g.24941283_24941306dup | NCBI36 |
NG_008281.1:g.7697_7720dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379044.5:c.743_766dup MANE Select | ENSP00000368332.4:p.Asp255_Ala256insGluGluGluLeuLeuGluAspAsp | |
ENST00000379044.4:c.743_766dup | ENSP00000368332.4:p.Asp255_Ala256insGluGluGluLeuLeuGluAspAsp | |
NM_139058.2:c.743_766dup | NP_620689.1:p.Asp255_Ala256insGluGluGluLeuLeuGluAspAsp | |
NM_139058.3:c.743_766dup MANE Select | NP_620689.1:p.Asp255_Ala256insGluGluGluLeuLeuGluAspAsp |