Linked Data
ClinVar Variation Id:
405324
dbSNP Id:
rs201829983
ExAC:
15:91334068 A / G
gnomAD v2:
15-91334068-A-G
gnomAD v3:
15-90790838-A-G
gnomAD v4:
15-90790838-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90790838A>G , CM000677.2:g.90790838A>G | GRCh38 |
| NC_000015.9:g.91334068A>G , CM000677.1:g.91334068A>G | GRCh37 |
| NC_000015.8:g.89135072A>G | NCBI36 |
| NG_007272.1:g.78467A>G , LRG_20:g.78467A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355112.8:c.3013A>G MANE Select | ENSP00000347232.3:p.Ile1005Val | |
| ENST00000560559.2:n.1586A>G | ||
| ENST00000648453.1:c.3013A>G | ENSP00000497646.1:p.Ile1005Val | |
| ENST00000680772.1:c.3013A>G | ENSP00000506117.1:p.Ile1005Val | |
| ENST00000681142.1:c.3013A>G | ENSP00000506682.1:p.Ile1005Val | |
| ENST00000355112.7:c.3013A>G | ENSP00000347232.3:p.Ile1005Val | |
| ENST00000559724.5:c.*1937A>G | ENSP00000453359.1:n.*1937A>G | |
| ENST00000560136.5:n.1039A>G | ||
| ENST00000560509.5:c.3013A>G | ENSP00000454158.1:p.Ile1005Val | |
| ENST00000560559.1:n.550A>G | ||
| NM_000057.3:c.3013A>G | NP_000048.1:p.Ile1005Val | |
| NM_001287246.1:c.3013A>G | NP_001274175.1:p.Ile1005Val | |
| NM_001287247.1:c.3013A>G | NP_001274176.1:p.Ile1005Val | |
| NM_001287248.1:c.1888A>G | NP_001274177.1:p.Ile630Val | |
| XM_006720632.2:c.1051A>G | XP_006720695.1:p.Ile351Val | |
| XM_011521881.1:c.1699A>G | XP_011520183.1:p.Ile567Val | |
| XM_011521881.2:c.1699A>G | XP_011520183.1:p.Ile567Val | |
| NM_000057.4:c.3013A>G MANE Select | NP_000048.1:p.Ile1005Val | |
| NM_001287246.2:c.3013A>G | NP_001274175.1:p.Ile1005Val | |
| NM_001287247.2:c.3013A>G | NP_001274176.1:p.Ile1005Val | |
| NM_001287248.2:c.1888A>G | NP_001274177.1:p.Ile630Val |