Linked Data
gnomAD v3:
19-38502822-C-CAGGGGCAGGGGGAGGGGGAGGGGG
gnomAD v4:
19-38502822-C-CAGGGGCAGGGGGAGGGGGAGGGGG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.38502830_38502831insGGGGAGGGGGAGGGGGAGGGGCAG , CM000681.2:g.38502830_38502831insGGGGAGGGGGAGGGGGAGGGGCAG | GRCh38 |
| NC_000019.9:g.38993470_38993471insGGGGAGGGGGAGGGGGAGGGGCAG , CM000681.1:g.38993470_38993471insGGGGAGGGGGAGGGGGAGGGGCAG | GRCh37 |
| NC_000019.8:g.43685310_43685311insGGGGAGGGGGAGGGGGAGGGGCAG | NCBI36 |
| NG_008866.1:g.74131_74132insGGGGAGGGGGAGGGGGAGGGGCAG , LRG_766:g.74131_74132insGGGGAGGGGGAGGGGGAGGGGCAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000599547.6:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | ENSP00000471601.2:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCA... | |
| ENST00000359596.8:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG MANE Select | ENSP00000352608.2:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCA... | |
| ENST00000355481.8:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | ENSP00000347667.3:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCA... | |
| ENST00000359596.7:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | ENSP00000352608.2:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCA... | |
| ENST00000360985.7:c.7833-50_7833-49insGGGGAGGGGGAGGGGGAGGGGCAG | ENSP00000354254.4:n.7833-50_7833-49insGGGGAGGGGGAGGGGGAGGGGCA... | |
| ENST00000594335.5:c.1288-50_1288-49insGGGGAGGGGGAGGGGGAGGGGCAG | ||
| NM_000540.2:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG , LRG_766t1:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | NP_000531.2:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| NM_001042723.1:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | NP_001036188.1:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| XM_006723317.1:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | XP_006723380.1:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| XM_006723319.1:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | XP_006723382.1:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| XM_011527204.1:c.7833-50_7833-49insGGGGAGGGGGAGGGGGAGGGGCAG | XP_011525506.1:n.7833-50_7833-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| XM_011527205.1:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | XP_011525507.1:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| XM_006723317.2:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | XP_006723380.1:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| XM_006723319.2:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | XP_006723382.1:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| XM_011527205.2:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | XP_011525507.1:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| XR_001753735.1:n.7919-50_7919-49insGGGGAGGGGGAGGGGGAGGGGCAG | ||
| NM_000540.3:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG MANE Select | NP_000531.2:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | |
| NM_001042723.2:c.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG | NP_001036188.1:n.7836-50_7836-49insGGGGAGGGGGAGGGGGAGGGGCAG |