HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863554del , CM000672.2:g.87863554del | GRCh38 |
NC_000010.10:g.89623311del , CM000672.1:g.89623311del | GRCh37 |
NC_000010.9:g.89613291del | NCBI36 |
NG_007466.2:g.5117del , LRG_311:g.5117del | |
NG_033079.1:g.4884del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-16-900del | ENSP00000516674.1:n.-16-900del | |
ENST00000688308.1:c.-17+441del | ENSP00000508752.1:n.-17+441del | |
ENST00000693560.1:c.-396del | ENSP00000509861.1:n.-396del | |
ENST00000371953.7:c.-916del | ENSP00000361021.3:n.-916del | |
ENST00000610634.1:c.-1018del | ENSP00000477517.1:n.-1018del | |
NM_000314.5:c.-915del | NP_000305.3:n.-915del | |
NM_000314.6:c.-915del | NP_000305.3:n.-915del | |
NM_001304717.2:c.-396del | NP_001291646.2:n.-396del | |
NM_001304718.1:c.-1620del | NP_001291647.1:n.-1620del |