HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863537del , CM000672.2:g.87863537del | GRCh38 |
NC_000010.10:g.89623294del , CM000672.1:g.89623294del | GRCh37 |
NC_000010.9:g.89613274del | NCBI36 |
NG_007466.2:g.5100del , LRG_311:g.5100del | |
NG_033079.1:g.4905del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+895del | ENSP00000516674.1:n.-17+895del | |
ENST00000688308.1:c.-17+424del | ENSP00000508752.1:n.-17+424del | |
ENST00000693560.1:c.-413del | ENSP00000509861.1:n.-413del | |
ENST00000371953.7:c.-933del | ENSP00000361021.3:n.-933del | |
ENST00000610634.1:c.-1035del | ENSP00000477517.1:n.-1035del | |
NM_000314.5:c.-932del | NP_000305.3:n.-932del | |
NM_000314.6:c.-932del | NP_000305.3:n.-932del | |
NM_001304717.2:c.-413del | NP_001291646.2:n.-413del | |
NM_001304718.1:c.-1637del | NP_001291647.1:n.-1637del |