Linked Data
dbSNP Id:
rs766837571
ExAC:
7:140476833 G / C
gnomAD v2:
7-140476833-G-C
gnomAD v4:
7-140777033-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.140777033G>C , CM000669.2:g.140777033G>C | GRCh38 |
| NC_000007.13:g.140476833G>C , CM000669.1:g.140476833G>C | GRCh37 |
| NC_000007.12:g.140123302G>C | NCBI36 |
| NG_007873.3:g.152732C>G , LRG_299:g.152732C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000646891.2:c.1573C>G MANE Select | ENSP00000493543.1:p.Leu525Val | |
| ENST00000288602.11:c.1693C>G | ENSP00000288602.7:p.Leu565Val | |
| ENST00000479537.6:c.243C>G | ||
| ENST00000496384.7:c.1573C>G | ENSP00000419060.2:p.Leu525Val | |
| ENST00000497784.2:c.*1023C>G | ENSP00000420119.2:n.*1023C>G | |
| ENST00000642228.1:c.*651C>G | ENSP00000493678.1:n.*651C>G | |
| ENST00000642875.1:n.1137C>G | ||
| ENST00000644120.1:n.1963C>G | ||
| ENST00000644650.1:c.669C>G | ||
| ENST00000644905.1:n.1662C>G | ||
| ENST00000644969.2:c.1693C>G MANE Plus Clinical | ENSP00000496776.1:p.Leu565Val | |
| ENST00000646730.1:c.1573C>G | ENSP00000494784.1:p.Leu525Val | |
| ENST00000646891.1:c.1573C>G | ENSP00000493543.1:p.Leu525Val | |
| ENST00000647434.1:c.616C>G | ENSP00000495132.1:p.Leu206Val | |
| ENST00000288602.10:c.1573C>G | ENSP00000288602.6:p.Leu525Val | |
| ENST00000496384.6:c.396C>G | ||
| ENST00000497784.1:c.1608C>G | ENSP00000420119.1:n.1608C>G | |
| NM_004333.4:c.1573C>G , LRG_299t1:c.1573C>G | NP_004324.2:p.Leu525Val | |
| XM_005250045.1:c.1573C>G | XP_005250102.1:p.Leu525Val | |
| XM_005250046.1:c.1573C>G | XP_005250103.1:p.Leu525Val | |
| XM_011516529.1:c.1573C>G | XP_011514831.1:p.Leu525Val | |
| XM_011516530.1:c.1573C>G | XP_011514832.1:p.Leu525Val | |
| XR_242190.1:n.1581C>G | ||
| XR_927520.1:n.1581C>G | ||
| XR_927521.1:n.1581C>G | ||
| XR_927522.1:n.1581C>G | ||
| XR_927523.1:n.1581C>G | ||
| NM_001354609.1:c.1573C>G | NP_001341538.1:p.Leu525Val | |
| NM_004333.5:c.1573C>G | NP_004324.2:p.Leu525Val | |
| NR_148928.1:n.1878C>G | ||
| XM_017012558.1:c.1693C>G | XP_016868047.1:p.Leu565Val | |
| XM_017012559.1:c.1693C>G | XP_016868048.1:p.Leu565Val | |
| XR_001744857.1:n.1701C>G | ||
| XR_001744858.1:n.1701C>G | ||
| NM_001354609.2:c.1573C>G | NP_001341538.1:p.Leu525Val | |
| NM_001374244.1:c.1693C>G | NP_001361173.1:p.Leu565Val | |
| NM_001374258.1:c.1693C>G MANE Plus Clinical | NP_001361187.1:p.Leu565Val | |
| NM_004333.6:c.1573C>G MANE Select | NP_004324.2:p.Leu525Val | |
| NM_001378467.1:c.1582C>G | NP_001365396.1:p.Leu528Val | |
| NM_001378468.1:c.1573C>G | NP_001365397.1:p.Leu525Val | |
| NM_001378469.1:c.1507C>G | NP_001365398.1:p.Leu503Val | |
| NM_001378470.1:c.1471C>G | NP_001365399.1:p.Leu491Val | |
| NM_001378471.1:c.1462C>G | NP_001365400.1:p.Leu488Val | |
| NM_001378472.1:c.1417C>G | NP_001365401.1:p.Leu473Val | |
| NM_001378473.1:c.1417C>G | NP_001365402.1:p.Leu473Val | |
| NM_001378474.1:c.1573C>G | NP_001365403.1:p.Leu525Val | |
| NM_001378475.1:c.1309C>G | NP_001365404.1:p.Leu437Val |