ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00061448 (EAS)
Genomes Max Group AF
0.00001972 (NFE)
Exomes Max Group AF
0.00067267 (EAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.36227295C>T , CM000671.2:g.36227295C>T | GRCh38 |
| NC_000009.11:g.36227292C>T , CM000671.1:g.36227292C>T | GRCh37 |
| NC_000009.10:g.36217292C>T | NCBI36 |
| NG_008246.1:g.54750G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396594.8:c.1327G>A (GNE) MANE Plus Clinical | ENSP00000379839.3:p.Val443Ile | |
| ENST00000543356.7:c.1057G>A (GNE) | ENSP00000437765.3:p.Val353Ile | |
| ENST00000642385.2:c.1234G>A (GNE) MANE Select | ENSP00000494141.2:p.Val412Ile | |
| ENST00000377902.5:c.1234G>A (GNE) | ENSP00000367134.4:p.Val412Ile | |
| ENST00000396594.7:c.1327G>A (GNE) | ENSP00000379839.3:p.Val443Ile | |
| ENST00000447283.6:c.1234G>A (GNE) | ENSP00000414760.2:p.Val412Ile | |
| ENST00000464497.5:c.485+23116C>T (CLTA) | ENSP00000419158.1:n.485+23116C>T | |
| ENST00000539208.5:c.904G>A (GNE) | ENSP00000445117.1:p.Val302Ile | |
| ENST00000539815.5:c.1234G>A (GNE) | ENSP00000439155.1:p.Val412Ile | |
| ENST00000543356.6:c.1219G>A (GNE) | ENSP00000437765.2:p.Val407Ile | |
| NM_001128227.2:c.1327G>A (GNE) | NP_001121699.1:p.Val443Ile | |
| NM_001190383.1:c.1234G>A (GNE) | NP_001177312.1:p.Val412Ile | |
| NM_001190384.1:c.904G>A (GNE) | NP_001177313.1:p.Val302Ile | |
| NM_001190388.1:c.1219G>A (GNE) | NP_001177317.1:p.Val407Ile | |
| NM_005476.5:c.1234G>A (GNE) | NP_005467.1:p.Val412Ile | |
| XM_005251334.3:c.1174G>A (GNE) | XP_005251391.1:p.Val392Ile | |
| NM_001190383.2:c.1234G>A (GNE) | NP_001177312.1:p.Val412Ile | |
| NM_001190384.2:c.904G>A (GNE) | NP_001177313.1:p.Val302Ile | |
| NM_005476.6:c.1234G>A (GNE) | NP_005467.1:p.Val412Ile | |
| XM_005251334.4:c.1174G>A (GNE) | XP_005251391.1:p.Val392Ile | |
| XM_017014167.1:c.1234G>A (GNE) | XP_016869656.1:p.Val412Ile | |
| XM_017014168.1:c.1081G>A (GNE) | XP_016869657.1:p.Val361Ile | |
| NM_001128227.3:c.1327G>A (GNE) MANE Plus Clinical | NP_001121699.1:p.Val443Ile | |
| NM_001190383.3:c.1234G>A (GNE) | NP_001177312.1:p.Val412Ile | |
| NM_001190384.3:c.904G>A (GNE) | NP_001177313.1:p.Val302Ile | |
| NM_001190388.2:c.1057G>A (GNE) | NP_001177317.2:p.Val353Ile | |
| NM_001374797.1:c.1081G>A (GNE) | NP_001361726.1:p.Val361Ile | |
| NM_001374798.1:c.1057G>A (GNE) | NP_001361727.1:p.Val353Ile | |
| NM_005476.7:c.1234G>A (GNE) MANE Select | NP_005467.1:p.Val412Ile |