HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085158_186085159insGGTA , CM000666.2:g.186085158_186085159insGGTA | GRCh38 |
NC_000004.11:g.187006312_187006313insGGTA , CM000666.1:g.187006312_187006313insGGTA | GRCh37 |
NC_000004.10:g.187243306_187243307insGGTA | NCBI36 |
NG_007278.1:g.21004_21005insGGTA , LRG_117:g.21004_21005insGGTA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000698352.1:c.*2552_*2553insGGTA | ENSP00000513675.1:n.*2552_*2553insGGTA | |
ENST00000698353.1:n.2875_2876insGGTA | ||
ENST00000698354.1:c.*285_*286insGGTA | ENSP00000513676.1:n.*285_*286insGGTA | |
ENST00000296795.8:c.*285_*286insGGTA MANE Select | ENSP00000296795.3:n.*285_*286insGGTA | |
ENST00000296795.7:c.*285_*286insGGTA | ENSP00000296795.2:n.*285_*286insGGTA | |
NM_003265.3:c.*285_*286insGGTA MANE Select | NP_003256.1:n.*285_*286insGGTA |