Linked Data
ClinVar Variation Id:
488581
ClinVar RCV Id:
RCV000578259
dbSNP Id:
rs777437871
ExAC:
9:134397529 C / T
gnomAD v2:
9-134397529-C-T
gnomAD v4:
9-131522142-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131522142C>T , CM000671.2:g.131522142C>T | GRCh38 |
| NC_000009.11:g.134397529C>T , CM000671.1:g.134397529C>T | GRCh37 |
| NC_000009.10:g.133387350C>T | NCBI36 |
| NG_008896.1:g.24241C>T | |
| NG_008896.2:g.24241C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000341012.13:c.1759C>T | ENSP00000343034.7:p.Leu587Phe | |
| ENST00000404875.7:n.2461C>T | ||
| ENST00000423007.6:c.1978C>T | ENSP00000404119.2:p.Leu660Phe | |
| ENST00000677295.2:c.*2265C>T | ENSP00000504346.2:n.*2265C>T | |
| ENST00000678264.2:c.*2104C>T | ENSP00000503157.2:n.*2104C>T | |
| ENST00000682070.1:n.2291-60C>T | ||
| ENST00000682813.1:n.2325C>T | ||
| ENST00000683392.1:n.4573-60C>T | ||
| ENST00000683712.1:n.2326C>T | ||
| ENST00000683900.1:n.3821C>T | ||
| ENST00000684062.1:n.2587C>T | ||
| ENST00000684579.1:n.3767C>T | ||
| ENST00000684679.1:n.1148C>T | ||
| ENST00000341012.12:c.1759C>T | ENSP00000343034.7:p.Leu587Phe | |
| ENST00000372220.5:c.790C>T | ENSP00000361294.5:p.Leu264Phe | |
| ENST00000372228.9:c.1987C>T | ENSP00000361302.3:p.Leu663Phe | |
| ENST00000402686.8:c.1921C>T MANE Select | ENSP00000385797.4:p.Leu641Phe | |
| ENST00000676640.1:c.1921C>T | ENSP00000503281.1:p.Leu641Phe | |
| ENST00000676803.1:c.982C>T | ENSP00000503093.1:p.Leu328Phe | |
| ENST00000676835.1:c.*1136C>T | ENSP00000502911.1:n.*1136C>T | |
| ENST00000677029.1:c.1465C>T | ENSP00000502936.1:p.Leu489Phe | |
| ENST00000677099.1:c.*1631C>T | ENSP00000504553.1:n.*1631C>T | |
| ENST00000677216.1:c.1570C>T | ENSP00000503772.1:p.Leu524Phe | |
| ENST00000677221.1:n.946C>T | ||
| ENST00000677295.1:c.*1203-60C>T | ENSP00000504346.1:n.*1203-60C>T | |
| ENST00000677444.1:c.1866C>T | ||
| ENST00000677586.1:n.1288C>T | ||
| ENST00000677626.1:c.1570C>T | ENSP00000503552.1:p.Leu524Phe | |
| ENST00000677853.1:c.*929C>T | ENSP00000503488.1:n.*929C>T | |
| ENST00000678202.1:n.1080C>T | ||
| ENST00000678264.1:c.*1298C>T | ENSP00000503157.1:n.*1298C>T | |
| ENST00000678303.1:c.1831C>T | ENSP00000503696.1:p.Leu611Phe | |
| ENST00000678366.1:c.*2170C>T | ENSP00000504353.1:n.*2170C>T | |
| ENST00000678546.1:c.*1866C>T | ENSP00000503062.1:n.*1866C>T | |
| ENST00000678548.1:c.*2060C>T | ENSP00000503934.1:n.*2060C>T | |
| ENST00000678626.1:n.1757C>T | ||
| ENST00000678739.1:c.*2147-60C>T | ENSP00000503806.1:n.*2147-60C>T | |
| ENST00000678833.1:c.*1673C>T | ENSP00000503893.1:n.*1673C>T | |
| ENST00000679023.1:c.1759C>T | ENSP00000503718.1:p.Leu587Phe | |
| ENST00000679076.1:c.1540C>T | ||
| ENST00000679111.1:c.*677C>T | ENSP00000504257.1:n.*677C>T | |
| ENST00000679189.1:c.1570C>T | ENSP00000503356.1:p.Leu524Phe | |
| ENST00000341012.11:c.1759C>T | ENSP00000343034.7:p.Leu587Phe | |
| ENST00000372220.4:c.784C>T | ENSP00000361294.4:p.Leu262Phe | |
| ENST00000372228.7:c.1987C>T | ENSP00000361302.3:p.Leu663Phe | |
| ENST00000402686.7:c.1921C>T | ENSP00000385797.3:p.Leu641Phe | |
| ENST00000404875.6:c.1570C>T | ENSP00000384531.2:p.Leu524Phe | |
| ENST00000423007.5:c.1921C>T | ENSP00000404119.1:p.Leu641Phe | |
| ENST00000485278.5:n.2471C>T | ||
| ENST00000494883.1:n.464C>T | ||
| NM_001077365.1:c.1921C>T | NP_001070833.1:p.Leu641Phe | |
| NM_001077366.1:c.1759C>T | NP_001070834.1:p.Leu587Phe | |
| NM_001136113.1:c.1921C>T | NP_001129585.1:p.Leu641Phe | |
| NM_001136114.1:c.1570C>T | NP_001129586.1:p.Leu524Phe | |
| NM_007171.3:c.1987C>T | NP_009102.3:p.Leu663Phe | |
| XM_005272156.1:c.1987C>T | XP_005272213.1:p.Leu663Phe | |
| XM_005272158.1:c.1825C>T | XP_005272215.1:p.Leu609Phe | |
| XM_005272159.1:c.1636C>T | XP_005272216.1:p.Leu546Phe | |
| XM_005272162.1:c.790C>T | XP_005272219.1:p.Leu264Phe | |
| XM_006716932.1:c.1636C>T | XP_006716995.1:p.Leu546Phe | |
| XM_011518140.1:c.1840C>T | XP_011516442.1:p.Leu614Phe | |
| XM_011518141.1:c.1774C>T | XP_011516443.1:p.Leu592Phe | |
| XM_011518142.1:c.1678C>T | XP_011516444.1:p.Leu560Phe | |
| XM_011518143.1:c.1672C>T | XP_011516445.1:p.Leu558Phe | |
| XM_011518145.1:c.1531C>T | XP_011516447.1:p.Leu511Phe | |
| XM_011518147.1:c.859C>T | XP_011516449.1:p.Leu287Phe | |
| XR_929703.1:n.2163C>T | ||
| NM_001353193.1:c.1987C>T | NP_001340122.1:p.Leu663Phe | |
| NM_001353194.1:c.1759C>T | NP_001340123.1:p.Leu587Phe | |
| NM_001353195.1:c.1570C>T | NP_001340124.1:p.Leu524Phe | |
| NM_001353196.1:c.1831C>T | NP_001340125.1:p.Leu611Phe | |
| NM_001353197.1:c.1825C>T | NP_001340126.1:p.Leu609Phe | |
| NM_001353198.1:c.1825C>T | NP_001340127.1:p.Leu609Phe | |
| NM_001353199.1:c.1636C>T | NP_001340128.1:p.Leu546Phe | |
| NM_001353200.1:c.1465C>T | NP_001340129.1:p.Leu489Phe | |
| NR_148391.1:n.1971C>T | ||
| NR_148392.1:n.2189C>T | ||
| NR_148393.1:n.2110C>T | ||
| NR_148394.1:n.1864C>T | ||
| NR_148395.1:n.2262C>T | ||
| NR_148396.1:n.1896C>T | ||
| NR_148397.1:n.2021C>T | ||
| NR_148398.1:n.1976C>T | ||
| NR_148399.1:n.2502C>T | ||
| NR_148400.1:n.2101C>T | ||
| XM_005272162.3:c.790C>T | XP_005272219.1:p.Leu264Phe | |
| XM_006716932.2:c.1636C>T | XP_006716995.1:p.Leu546Phe | |
| XM_011518140.2:c.1840C>T | XP_011516442.1:p.Leu614Phe | |
| XM_011518141.2:c.1774C>T | XP_011516443.1:p.Leu592Phe | |
| XM_011518142.2:c.1678C>T | XP_011516444.1:p.Leu560Phe | |
| XM_011518143.2:c.1672C>T | XP_011516445.1:p.Leu558Phe | |
| XM_011518145.2:c.1531C>T | XP_011516447.1:p.Leu511Phe | |
| XM_017014205.2:c.790C>T | XP_016869694.1:p.Leu264Phe | |
| XM_024447380.1:c.790C>T | XP_024303148.1:p.Leu264Phe | |
| XM_024447381.1:c.1096C>T | XP_024303149.1:p.Leu366Phe | |
| XM_024447382.1:c.790C>T | XP_024303150.1:p.Leu264Phe | |
| XR_001746160.2:n.2091C>T | ||
| XR_001746162.2:n.2296C>T | ||
| XR_001746164.1:n.2013C>T | ||
| XR_001746166.2:n.2308C>T | ||
| NM_001077365.2:c.1921C>T MANE Select | NP_001070833.1:p.Leu641Phe | |
| NM_001077366.2:c.1759C>T | NP_001070834.1:p.Leu587Phe | |
| NM_001136113.2:c.1921C>T | NP_001129585.1:p.Leu641Phe | |
| NM_001136114.2:c.1570C>T | NP_001129586.1:p.Leu524Phe | |
| NM_001353193.2:c.1987C>T | NP_001340122.2:p.Leu663Phe | |
| NM_001353194.2:c.1759C>T | NP_001340123.1:p.Leu587Phe | |
| NM_001353195.2:c.1570C>T | NP_001340124.1:p.Leu524Phe | |
| NM_001353196.2:c.1831C>T | NP_001340125.1:p.Leu611Phe | |
| NM_001353197.2:c.1825C>T | NP_001340126.2:p.Leu609Phe | |
| NM_001353198.2:c.1825C>T | NP_001340127.2:p.Leu609Phe | |
| NM_001353199.2:c.1636C>T | NP_001340128.2:p.Leu546Phe | |
| NM_001353200.2:c.1465C>T | NP_001340129.1:p.Leu489Phe | |
| NM_001374689.1:c.1909C>T | NP_001361618.1:p.Leu637Phe | |
| NM_001374690.1:c.1702C>T | NP_001361619.1:p.Leu568Phe | |
| NM_001374691.1:c.1570C>T | NP_001361620.1:p.Leu524Phe | |
| NM_001374692.1:c.1570C>T | NP_001361621.1:p.Leu524Phe | |
| NM_001374693.1:c.1570C>T | NP_001361622.1:p.Leu524Phe | |
| NM_001374695.1:c.1531C>T | NP_001361624.1:p.Leu511Phe | |
| NM_007171.4:c.1987C>T | NP_009102.4:p.Leu663Phe | |
| NR_148391.2:n.1955C>T | ||
| NR_148392.2:n.2173C>T | ||
| NR_148393.2:n.2094C>T | ||
| NR_148394.2:n.1848C>T | ||
| NR_148395.2:n.2246C>T | ||
| NR_148396.2:n.1880C>T | ||
| NR_148397.2:n.2005C>T | ||
| NR_148398.2:n.1960C>T | ||
| NR_148399.2:n.2486C>T | ||
| NR_148400.2:n.2085C>T |