HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085490del , CM000666.2:g.186085490del | GRCh38 |
NC_000004.11:g.187006644del , CM000666.1:g.187006644del | GRCh37 |
NC_000004.10:g.187243638del | NCBI36 |
NG_007278.1:g.21336del , LRG_117:g.21336del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000698352.1:c.*2884del | ENSP00000513675.1:n.*2884del | |
ENST00000698353.1:n.3207del | ||
ENST00000698354.1:c.*617del | ENSP00000513676.1:n.*617del | |
ENST00000296795.8:c.*617del MANE Select | ENSP00000296795.3:n.*617del | |
ENST00000296795.7:c.*617del | ENSP00000296795.2:n.*617del | |
NM_003265.3:c.*617del MANE Select | NP_003256.1:n.*617del |