HGVS | Genome Assembly |
---|---|
NC_000004.12:g.186085625del , CM000666.2:g.186085625del | GRCh38 |
NC_000004.11:g.187006779del , CM000666.1:g.187006779del | GRCh37 |
NC_000004.10:g.187243773del | NCBI36 |
NG_007278.1:g.21471del , LRG_117:g.21471del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000698352.1:c.*3019del | ENSP00000513675.1:n.*3019del | |
ENST00000698353.1:n.3342del | ||
ENST00000698354.1:c.*752del | ENSP00000513676.1:n.*752del | |
ENST00000296795.8:c.*752del MANE Select | ENSP00000296795.3:n.*752del | |
ENST00000296795.7:c.*752del | ENSP00000296795.2:n.*752del | |
NM_003265.3:c.*752del MANE Select | NP_003256.1:n.*752del |