HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717811_12717814del , CM000674.2:g.12717811_12717814del | GRCh38 |
NC_000012.11:g.12870745_12870748del , CM000674.1:g.12870745_12870748del | GRCh37 |
NC_000012.10:g.12762012_12762015del | NCBI36 |
NG_016341.1:g.5444_5447del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614874.2:c.-29_-26del | ENSP00000507272.1:n.-29_-26del | |
ENST00000682620.1:n.1631-1014_1631-1011del | ||
ENST00000684771.1:n.585-1014_585-1011del | ||
ENST00000228872.9:c.-29_-26del MANE Select | ENSP00000228872.4:n.-29_-26del | |
ENST00000228872.8:c.-29_-26del | ENSP00000228872.4:n.-29_-26del | |
ENST00000477087.1:n.155-1014_155-1011del | ||
NM_004064.4:c.-29_-26del | NP_004055.1:n.-29_-26del | |
NM_004064.5:c.-29_-26del MANE Select | NP_004055.1:n.-29_-26del |