HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717786_12717795del , CM000674.2:g.12717786_12717795del | GRCh38 |
NC_000012.11:g.12870720_12870729del , CM000674.1:g.12870720_12870729del | GRCh37 |
NC_000012.10:g.12761987_12761996del | NCBI36 |
NG_016341.1:g.5419_5428del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614874.2:c.-54_-45del | ENSP00000507272.1:n.-54_-45del | |
ENST00000682620.1:n.1631-1039_1631-1030del | ||
ENST00000684771.1:n.585-1039_585-1030del | ||
ENST00000228872.9:c.-54_-45del MANE Select | ENSP00000228872.4:n.-54_-45del | |
ENST00000228872.8:c.-54_-45del | ENSP00000228872.4:n.-54_-45del | |
ENST00000477087.1:n.155-1039_155-1030del | ||
NM_004064.4:c.-54_-45del | NP_004055.1:n.-54_-45del | |
NM_004064.5:c.-54_-45del MANE Select | NP_004055.1:n.-54_-45del |