HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94989069del , CM000672.2:g.94989069del | GRCh38 |
NC_000010.10:g.96748826del , CM000672.1:g.96748826del | GRCh37 |
NC_000010.9:g.96738816del | NCBI36 |
NG_008385.1:g.55412del | |
NG_008385.2:g.55912del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.*41del MANE Select | ENSP00000260682.6:n.*41del | |
ENST00000643112.1:c.*523del | ENSP00000496202.1:n.*523del | |
ENST00000260682.6:c.*41del | ENSP00000260682.6:n.*41del | |
NM_000771.3:c.*41del | NP_000762.2:n.*41del | |
NM_000771.4:c.*41del MANE Select | NP_000762.2:n.*41del |