HGVS | Genome Assembly |
---|---|
NC_000016.10:g.82148515_82148517delinsAGG , CM000678.2:g.82148515_82148517delinsAGG | GRCh38 |
NC_000016.9:g.82182120_82182122delinsAGG , CM000678.1:g.82182120_82182122delinsAGG | GRCh37 |
NC_000016.8:g.80739621_80739623delinsAGG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000258169.9:c.*214_*216delinsCCT MANE Select | ENSP00000258169.4:n.*214_*216delinsCCT | |
ENST00000258169.8:c.*214_*216delinsCCT | ENSP00000258169.4:n.*214_*216delinsCCT | |
ENST00000563100.5:c.*72+142_*72+144delinsCCT | ENSP00000454996.1:n.*72+142_*72+144delinsCCT | |
NM_005792.2:c.*214_*216delinsCCT MANE Select | NP_005783.2:n.*214_*216delinsCCT | |
XM_011522808.1:c.*214_*216delinsCCT | XP_011521110.1:n.*214_*216delinsCCT | |
XM_011522808.3:c.*214_*216delinsCCT | XP_011521110.1:n.*214_*216delinsCCT |