HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74751907_74751908insGAACCAGAAC , CM000677.2:g.74751907_74751908insGAACCAGAAC | GRCh38 |
NC_000015.9:g.75044248_75044249insGAACCAGAAC , CM000677.1:g.75044248_75044249insGAACCAGAAC | GRCh37 |
NC_000015.8:g.72831301_72831302insGAACCAGAAC | NCBI36 |
NG_008431.1:g.34366_34367insGAACCAGAAC | |
NG_008431.2:g.34366_34367insGAACCAGAAC | |
NG_061543.1:g.8063_8064insGAACCAGAAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000343932.5:c.1042+53_1042+54insGAACCAGAAC MANE Select | ENSP00000342007.4:n.1042+53_1042+54insGAACCAGAAC | |
ENST00000343932.4:c.1042+53_1042+54insGAACCAGAAC | ENSP00000342007.4:n.1042+53_1042+54insGAACCAGAAC | |
NM_000761.4:c.1042+53_1042+54insGAACCAGAAC | NP_000752.2:n.1042+53_1042+54insGAACCAGAAC | |
NM_000761.5:c.1042+53_1042+54insGAACCAGAAC MANE Select | NP_000752.2:n.1042+53_1042+54insGAACCAGAAC |