HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863547del , CM000672.2:g.87863547del | GRCh38 |
NC_000010.10:g.89623304del , CM000672.1:g.89623304del | GRCh37 |
NC_000010.9:g.89613284del | NCBI36 |
NG_007466.2:g.5110del , LRG_311:g.5110del | |
NG_033079.1:g.4892del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+905del | ENSP00000516674.1:n.-17+905del | |
ENST00000688308.1:c.-17+434del | ENSP00000508752.1:n.-17+434del | |
ENST00000693560.1:c.-403del | ENSP00000509861.1:n.-403del | |
ENST00000371953.7:c.-923del | ENSP00000361021.3:n.-923del | |
ENST00000610634.1:c.-1025del | ENSP00000477517.1:n.-1025del | |
NM_000314.5:c.-922del | NP_000305.3:n.-922del | |
NM_000314.6:c.-922del | NP_000305.3:n.-922del | |
NM_001304717.2:c.-403del | NP_001291646.2:n.-403del | |
NM_001304718.1:c.-1627del | NP_001291647.1:n.-1627del |