Linked Data
ClinVar Variation Id:
366797
dbSNP Id:
rs140396892
gnomAD v2:
9-36214573-C-T
gnomAD v3:
9-36214576-C-T
gnomAD v4:
9-36214576-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.36214576C>T , CM000671.2:g.36214576C>T | GRCh38 |
| NC_000009.11:g.36214573C>T , CM000671.1:g.36214573C>T | GRCh37 |
| NC_000009.10:g.36204573C>T | NCBI36 |
| NG_008246.1:g.67469G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396594.8:c.*2789G>A (GNE) MANE Plus Clinical | ENSP00000379839.3:n.*2789G>A | |
| ENST00000642385.2:c.*2789G>A (GNE) MANE Select | ENSP00000494141.2:n.*2789G>A | |
| ENST00000396594.7:c.*2789G>A (GNE) | ENSP00000379839.3:n.*2789G>A | |
| ENST00000464497.5:c.485+10397C>T (CLTA) | ENSP00000419158.1:n.485+10397C>T | |
| ENST00000539815.5:c.*1315G>A (GNE) | ENSP00000439155.1:n.*1315G>A | |
| NM_001128227.2:c.*2789G>A (GNE) | NP_001121699.1:n.*2789G>A | |
| NM_001190383.1:c.*2789G>A (GNE) | NP_001177312.1:n.*2789G>A | |
| NM_001190384.1:c.*2789G>A (GNE) | NP_001177313.1:n.*2789G>A | |
| NM_001190388.1:c.*2789G>A (GNE) | NP_001177317.1:n.*2789G>A | |
| NM_005476.5:c.*2789G>A (GNE) | NP_005467.1:n.*2789G>A | |
| NM_001190383.2:c.*2789G>A (GNE) | NP_001177312.1:n.*2789G>A | |
| NM_001190384.2:c.*2789G>A (GNE) | NP_001177313.1:n.*2789G>A | |
| NM_005476.6:c.*2789G>A (GNE) | NP_005467.1:n.*2789G>A | |
| XM_017014167.1:c.*2789G>A (GNE) | XP_016869656.1:n.*2789G>A | |
| NM_001128227.3:c.*2789G>A (GNE) MANE Plus Clinical | NP_001121699.1:n.*2789G>A | |
| NM_001190383.3:c.*2789G>A (GNE) | NP_001177312.1:n.*2789G>A | |
| NM_001190384.3:c.*2789G>A (GNE) | NP_001177313.1:n.*2789G>A | |
| NM_001190388.2:c.*2789G>A (GNE) | NP_001177317.2:n.*2789G>A | |
| NM_001374797.1:c.*2789G>A (GNE) | NP_001361726.1:n.*2789G>A | |
| NM_001374798.1:c.*2789G>A (GNE) | NP_001361727.1:n.*2789G>A | |
| NM_005476.7:c.*2789G>A (GNE) MANE Select | NP_005467.1:n.*2789G>A |