HGVS | Genome Assembly |
---|---|
NC_000020.11:g.3082906_3082911delinsCGCAGG , CM000682.2:g.3082906_3082911delinsCGCAGG | GRCh38 |
NC_000020.10:g.3063552_3063557delinsCGCAGG , CM000682.1:g.3063552_3063557delinsCGCAGG | GRCh37 |
NC_000020.9:g.3011552_3011557delinsCGCAGG | NCBI36 |
NG_008663.1:g.6814_6819delinsCCTGCG , LRG_715:g.6814_6819delinsCCTGCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380293.3:c.322+66_322+71delinsCCTGCG MANE Select | ENSP00000369647.3:n.322+66_322+71delinsCCTGCG | |
NM_000490.4:c.322+66_322+71delinsCCTGCG , LRG_715t1:c.322+66_322+71delinsCCTGCG | NP_000481.2:n.322+66_322+71delinsCCTGCG | |
XM_011529267.1:c.322+66_322+71delinsCCTGCG | XP_011527569.1:n.322+66_322+71delinsCCTGCG | |
XM_011529267.2:c.322+66_322+71delinsCCTGCG | XP_011527569.1:n.322+66_322+71delinsCCTGCG | |
NM_000490.5:c.322+66_322+71delinsCCTGCG MANE Select | NP_000481.2:n.322+66_322+71delinsCCTGCG |