Linked Data
ClinVar Variation Id:
50559
ClinVar RCV Id:
RCV000043550
dbSNP Id:
rs397515443
PubMed:
PMID:21753178
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.74364111C>T , CM000670.2:g.74364111C>T | GRCh38 |
| NC_000008.10:g.75276346C>T , CM000670.1:g.75276346C>T | GRCh37 |
| NC_000008.9:g.75438901C>T | NCBI36 |
| NG_008787.2:g.47982C>T | |
| NG_008787.3:g.47982C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000220822.12:c.821C>T MANE Select | ENSP00000220822.7:p.Pro274Leu | |
| ENST00000434412.3:c.689C>T | ENSP00000417006.3:p.Pro230Leu | |
| ENST00000520797.6:n.932C>T | ||
| ENST00000521096.6:n.677C>T | ||
| ENST00000522568.2:c.*493C>T | ENSP00000430136.1:n.*493C>T | |
| ENST00000523640.2:c.165+12790C>T | ENSP00000502017.1:n.165+12790C>T | |
| ENST00000524195.2:c.280+1058C>T | ENSP00000502308.1:n.280+1058C>T | |
| ENST00000674612.1:c.494C>T | ENSP00000501864.1:p.Pro165Leu | |
| ENST00000674710.1:c.694+1058C>T | ENSP00000502762.1:n.694+1058C>T | |
| ENST00000674754.1:c.*2384C>T | ENSP00000502063.1:n.*2384C>T | |
| ENST00000674756.1:c.*366+1058C>T | ENSP00000501860.1:n.*366+1058C>T | |
| ENST00000674806.1:c.494C>T | ENSP00000502637.1:p.Pro165Leu | |
| ENST00000674865.1:c.617C>T | ENSP00000502437.1:p.Pro206Leu | |
| ENST00000674926.1:c.*1453C>T | ENSP00000501799.1:n.*1453C>T | |
| ENST00000674934.1:c.*509C>T | ENSP00000502187.1:n.*509C>T | |
| ENST00000674944.1:c.*1424C>T | ENSP00000501858.1:n.*1424C>T | |
| ENST00000674946.1:c.694+1058C>T | ENSP00000501569.1:n.694+1058C>T | |
| ENST00000674973.1:c.515C>T | ENSP00000502447.1:p.Pro172Leu | |
| ENST00000675007.1:c.*559C>T | ENSP00000502119.1:n.*559C>T | |
| ENST00000675060.1:c.*486C>T | ENSP00000501616.1:n.*486C>T | |
| ENST00000675165.1:c.818C>T | ENSP00000502612.1:p.Pro273Leu | |
| ENST00000675220.1:c.494C>T | ENSP00000502588.1:p.Pro165Leu | |
| ENST00000675265.1:c.*571C>T | ENSP00000501848.1:n.*571C>T | |
| ENST00000675336.1:c.*307C>T | ENSP00000502120.1:n.*307C>T | |
| ENST00000675376.1:c.494C>T | ENSP00000502838.1:p.Pro165Leu | |
| ENST00000675463.1:c.899C>T | ENSP00000502327.1:p.Pro300Leu | |
| ENST00000675472.1:c.*307C>T | ENSP00000501946.1:n.*307C>T | |
| ENST00000675474.1:n.406C>T | ||
| ENST00000675560.1:c.*366+1058C>T | ENSP00000502118.1:n.*366+1058C>T | |
| ENST00000675625.1:c.*493C>T | ENSP00000501626.1:n.*493C>T | |
| ENST00000675633.1:c.*228C>T | ENSP00000501785.1:n.*228C>T | |
| ENST00000675661.1:c.*581C>T | ENSP00000501958.1:n.*581C>T | |
| ENST00000675706.1:n.2779C>T | ||
| ENST00000675821.1:c.494C>T | ENSP00000502198.1:p.Pro165Leu | |
| ENST00000675832.1:c.*493C>T | ENSP00000502041.1:n.*493C>T | |
| ENST00000675928.1:c.647C>T | ENSP00000501568.1:p.Pro216Leu | |
| ENST00000675944.1:c.617C>T | ENSP00000502673.1:p.Pro206Leu | |
| ENST00000675999.1:c.694+1058C>T | ENSP00000502572.1:n.694+1058C>T | |
| ENST00000676049.1:c.*723C>T | ENSP00000501912.1:n.*723C>T | |
| ENST00000676112.1:c.887C>T | ENSP00000502295.1:p.Pro296Leu | |
| ENST00000676143.1:c.494C>T | ENSP00000502828.1:p.Pro165Leu | |
| ENST00000676207.1:c.694+1058C>T | ENSP00000502638.1:n.694+1058C>T | |
| ENST00000676377.1:c.494C>T | ENSP00000502756.1:p.Pro165Leu | |
| ENST00000676415.1:c.*127C>T | ENSP00000502665.1:n.*127C>T | |
| ENST00000676443.1:c.773C>T | ENSP00000501769.1:p.Pro258Leu | |
| ENST00000220822.11:c.821C>T | ENSP00000220822.7:p.Pro274Leu | |
| ENST00000434412.2:c.617C>T | ENSP00000417006.2:p.Pro206Leu | |
| ENST00000520797.5:n.586C>T | ||
| ENST00000521096.5:n.627C>T | ||
| ENST00000522568.1:c.*493C>T | ENSP00000430136.1:n.*493C>T | |
| ENST00000524195.1:n.103+1058C>T | ||
| NM_001040875.2:c.617C>T | NP_001035808.1:p.Pro206Leu | |
| NM_018972.2:c.821C>T | NP_061845.2:p.Pro274Leu | |
| NR_046346.1:n.755C>T | ||
| XM_011517551.1:c.1115C>T | XP_011515853.1:p.Pro372Leu | |
| XM_011517552.1:c.494C>T | XP_011515854.1:p.Pro165Leu | |
| NM_001040875.3:c.617C>T | NP_001035808.1:p.Pro206Leu | |
| NM_001362929.1:c.494C>T | NP_001349858.1:p.Pro165Leu | |
| NM_001362930.1:c.647C>T | NP_001349859.1:p.Pro216Leu | |
| NM_001362931.1:c.694+1058C>T | NP_001349860.1:n.694+1058C>T | |
| NM_001362932.1:c.494C>T | NP_001349861.1:p.Pro165Leu | |
| NM_018972.3:c.821C>T | NP_061845.2:p.Pro274Leu | |
| NM_001362931.2:c.694+1058C>T | NP_001349860.1:n.694+1058C>T | |
| NM_018972.4:c.821C>T MANE Select | NP_061845.2:p.Pro274Leu | |
| NM_001040875.4:c.617C>T | NP_001035808.1:p.Pro206Leu | |
| NM_001362929.2:c.494C>T | NP_001349858.1:p.Pro165Leu | |
| NM_001362930.2:c.647C>T | NP_001349859.1:p.Pro216Leu | |
| NM_001362932.2:c.494C>T | NP_001349861.1:p.Pro165Leu |