HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20425277_20425301del , CM000684.2:g.20425277_20425301del | GRCh38 |
NC_000022.10:g.20779567_20779591del , CM000684.1:g.20779567_20779591del | GRCh37 |
NC_000022.9:g.19109567_19109591del | NCBI36 |
NG_031868.2:g.17567_17591del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000622235.5:c.*82_*106del MANE Select | ENSP00000477564.2:n.*82_*106del | |
ENST00000615031.4:c.*82_*106del | ENSP00000479389.1:n.*82_*106del | |
ENST00000622235.4:c.*82_*106del | ENSP00000477564.1:n.*82_*106del | |
ENST00000623402.1:c.*82_*106del | ENSP00000485276.1:n.*82_*106del | |
NM_153334.6:c.*82_*106del | NP_699165.3:n.*82_*106del | |
NM_182895.4:c.*82_*106del | NP_878315.2:n.*82_*106del | |
NM_153334.7:c.*82_*106del | NP_699165.3:n.*82_*106del | |
NM_182895.5:c.*82_*106del MANE Select | NP_878315.2:n.*82_*106del |