Linked Data
ClinVar Variation Id:
284451
ClinVar RCV Id:
RCV000277347
RCV000298514
RCV000343980
RCV000353363
RCV000533442
RCV003977768
RCV003387823
dbSNP Id:
rs35638832
ExAC:
9:36227259 T / C
gnomAD v2:
9-36227259-T-C
gnomAD v3:
9-36227262-T-C
gnomAD v4:
9-36227262-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.36227262T>C , CM000671.2:g.36227262T>C | GRCh38 |
| NC_000009.11:g.36227259T>C , CM000671.1:g.36227259T>C | GRCh37 |
| NC_000009.10:g.36217259T>C | NCBI36 |
| NG_008246.1:g.54783A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396594.8:c.1360A>G (GNE) MANE Plus Clinical | ENSP00000379839.3:p.Ile454Val | |
| ENST00000543356.7:c.1090A>G (GNE) | ENSP00000437765.3:p.Ile364Val | |
| ENST00000642385.2:c.1267A>G (GNE) MANE Select | ENSP00000494141.2:p.Ile423Val | |
| ENST00000377902.5:c.1267A>G (GNE) | ENSP00000367134.4:p.Ile423Val | |
| ENST00000396594.7:c.1360A>G (GNE) | ENSP00000379839.3:p.Ile454Val | |
| ENST00000447283.6:c.1267A>G (GNE) | ENSP00000414760.2:p.Ile423Val | |
| ENST00000464497.5:c.485+23083T>C (CLTA) | ENSP00000419158.1:n.485+23083T>C | |
| ENST00000539208.5:c.937A>G (GNE) | ENSP00000445117.1:p.Ile313Val | |
| ENST00000539815.5:c.1267A>G (GNE) | ENSP00000439155.1:p.Ile423Val | |
| ENST00000543356.6:c.1252A>G (GNE) | ENSP00000437765.2:p.Ile418Val | |
| NM_001128227.2:c.1360A>G (GNE) | NP_001121699.1:p.Ile454Val | |
| NM_001190383.1:c.1267A>G (GNE) | NP_001177312.1:p.Ile423Val | |
| NM_001190384.1:c.937A>G (GNE) | NP_001177313.1:p.Ile313Val | |
| NM_001190388.1:c.1252A>G (GNE) | NP_001177317.1:p.Ile418Val | |
| NM_005476.5:c.1267A>G (GNE) | NP_005467.1:p.Ile423Val | |
| XM_005251334.3:c.1207A>G (GNE) | XP_005251391.1:p.Ile403Val | |
| NM_001190383.2:c.1267A>G (GNE) | NP_001177312.1:p.Ile423Val | |
| NM_001190384.2:c.937A>G (GNE) | NP_001177313.1:p.Ile313Val | |
| NM_005476.6:c.1267A>G (GNE) | NP_005467.1:p.Ile423Val | |
| XM_005251334.4:c.1207A>G (GNE) | XP_005251391.1:p.Ile403Val | |
| XM_017014167.1:c.1267A>G (GNE) | XP_016869656.1:p.Ile423Val | |
| XM_017014168.1:c.1114A>G (GNE) | XP_016869657.1:p.Ile372Val | |
| NM_001128227.3:c.1360A>G (GNE) MANE Plus Clinical | NP_001121699.1:p.Ile454Val | |
| NM_001190383.3:c.1267A>G (GNE) | NP_001177312.1:p.Ile423Val | |
| NM_001190384.3:c.937A>G (GNE) | NP_001177313.1:p.Ile313Val | |
| NM_001190388.2:c.1090A>G (GNE) | NP_001177317.2:p.Ile364Val | |
| NM_001374797.1:c.1114A>G (GNE) | NP_001361726.1:p.Ile372Val | |
| NM_001374798.1:c.1090A>G (GNE) | NP_001361727.1:p.Ile364Val | |
| NM_005476.7:c.1267A>G (GNE) MANE Select | NP_005467.1:p.Ile423Val |