Linked Data
ClinVar Variation Id:
587514
ClinVar RCV Id:
RCV000714710
dbSNP Id:
rs1562957000
gnomAD v4:
7-140781621-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140781621T>C , CM000669.2:g.140781621T>C | GRCh38 |
| NC_000007.13:g.140481421T>C , CM000669.1:g.140481421T>C | GRCh37 |
| NC_000007.12:g.140127890T>C | NCBI36 |
| NG_007873.3:g.148144A>G , LRG_299:g.148144A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000646891.2:c.1387A>G MANE Select | ENSP00000493543.1:p.Ile463Val | |
| ENST00000288602.11:c.1507A>G | ENSP00000288602.7:p.Ile503Val | |
| ENST00000479537.6:c.57A>G | ||
| ENST00000496384.7:c.1387A>G | ENSP00000419060.2:p.Ile463Val | |
| ENST00000497784.2:c.*837A>G | ENSP00000420119.2:n.*837A>G | |
| ENST00000642228.1:c.*465A>G | ENSP00000493678.1:n.*465A>G | |
| ENST00000642875.1:n.829A>G | ||
| ENST00000644120.1:n.1777A>G | ||
| ENST00000644650.1:c.483A>G | ||
| ENST00000644905.1:n.1476A>G | ||
| ENST00000644969.2:c.1507A>G MANE Plus Clinical | ENSP00000496776.1:p.Ile503Val | |
| ENST00000646334.1:n.517A>G | ||
| ENST00000646730.1:c.1387A>G | ENSP00000494784.1:p.Ile463Val | |
| ENST00000646891.1:c.1387A>G | ENSP00000493543.1:p.Ile463Val | |
| ENST00000647434.1:c.430A>G | ENSP00000495132.1:p.Ile144Val | |
| ENST00000288602.10:c.1387A>G | ENSP00000288602.6:p.Ile463Val | |
| ENST00000496384.6:c.210A>G | ||
| ENST00000497784.1:c.1422A>G | ENSP00000420119.1:n.1422A>G | |
| NM_004333.4:c.1387A>G , LRG_299t1:c.1387A>G | NP_004324.2:p.Ile463Val | |
| XM_005250045.1:c.1387A>G | XP_005250102.1:p.Ile463Val | |
| XM_005250046.1:c.1387A>G | XP_005250103.1:p.Ile463Val | |
| XM_011516529.1:c.1387A>G | XP_011514831.1:p.Ile463Val | |
| XM_011516530.1:c.1387A>G | XP_011514832.1:p.Ile463Val | |
| XR_242190.1:n.1395A>G | ||
| XR_927520.1:n.1395A>G | ||
| XR_927521.1:n.1395A>G | ||
| XR_927522.1:n.1395A>G | ||
| XR_927523.1:n.1395A>G | ||
| NM_001354609.1:c.1387A>G | NP_001341538.1:p.Ile463Val | |
| NM_004333.5:c.1387A>G | NP_004324.2:p.Ile463Val | |
| NR_148928.1:n.1692A>G | ||
| XM_017012558.1:c.1507A>G | XP_016868047.1:p.Ile503Val | |
| XM_017012559.1:c.1507A>G | XP_016868048.1:p.Ile503Val | |
| XR_001744857.1:n.1515A>G | ||
| XR_001744858.1:n.1515A>G | ||
| NM_001354609.2:c.1387A>G | NP_001341538.1:p.Ile463Val | |
| NM_001374244.1:c.1507A>G | NP_001361173.1:p.Ile503Val | |
| NM_001374258.1:c.1507A>G MANE Plus Clinical | NP_001361187.1:p.Ile503Val | |
| NM_004333.6:c.1387A>G MANE Select | NP_004324.2:p.Ile463Val | |
| NM_001378467.1:c.1396A>G | NP_001365396.1:p.Ile466Val | |
| NM_001378468.1:c.1387A>G | NP_001365397.1:p.Ile463Val | |
| NM_001378469.1:c.1321A>G | NP_001365398.1:p.Ile441Val | |
| NM_001378470.1:c.1285A>G | NP_001365399.1:p.Ile429Val | |
| NM_001378471.1:c.1276A>G | NP_001365400.1:p.Ile426Val | |
| NM_001378472.1:c.1231A>G | NP_001365401.1:p.Ile411Val | |
| NM_001378473.1:c.1231A>G | NP_001365402.1:p.Ile411Val | |
| NM_001378474.1:c.1387A>G | NP_001365403.1:p.Ile463Val | |
| NM_001378475.1:c.1123A>G | NP_001365404.1:p.Ile375Val |