HGVS | Genome Assembly |
---|---|
NC_000015.10:g.65077613_65077614insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG , CM000677.2:g.65077613_65077614insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG | GRCh38 |
NC_000015.9:g.65369951_65369952insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG , CM000677.1:g.65369951_65369952insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG | GRCh37 |
NC_000015.8:g.63157004_63157005insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG | NCBI36 |
NG_021411.1:g.5798_5799insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG , LRG_682:g.5798_5799insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000432196.5:c.798_799insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG MANE Select | ENSP00000388723.2:p.Glu266_Phe267insGluAs... | |
ENST00000432196.3:c.798_799insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG | ENSP00000388723.2:p.Glu266_Phe267insGluAs... | |
NM_001101362.2:c.798_799insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG , LRG_682t1:c.798_799insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG | NP_001094832.1:p.Glu266_Phe267insGluAspAl... | |
NM_001101362.3:c.798_799insGAGGACGCCCATCAGCAACTCTACGCCATCGGCGGCGAG MANE Select | NP_001094832.1:p.Glu266_Phe267insGluAspAl... |