Linked Data
ClinVar Variation Id:
365031
dbSNP Id:
rs139344911
ExAC:
9:130258316 C / T
gnomAD v2:
9-130258316-C-T
gnomAD v3:
9-127496037-C-T
gnomAD v4:
9-127496037-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127496037C>T , CM000671.2:g.127496037C>T | GRCh38 |
| NC_000009.11:g.130258316C>T , CM000671.1:g.130258316C>T | GRCh37 |
| NC_000009.10:g.129298137C>T | NCBI36 |
| NG_032008.1:g.49552C>T , LRG_373:g.49552C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300417.11:c.1772C>T MANE Select | ENSP00000300417.6:p.Ala591Val | |
| ENST00000472068.2:c.*1496C>T | ENSP00000501555.1:n.*1496C>T | |
| ENST00000483302.6:n.2437C>T | ||
| ENST00000498513.6:c.*663C>T | ENSP00000501637.1:n.*663C>T | |
| ENST00000674511.1:n.1371C>T | ||
| ENST00000674516.1:c.1772C>T | ENSP00000502441.1:p.Ala591Val | |
| ENST00000674621.1:n.1822C>T | ||
| ENST00000674771.1:c.*415C>T | ENSP00000502627.1:n.*415C>T | |
| ENST00000674784.1:c.*832C>T | ENSP00000501837.1:n.*832C>T | |
| ENST00000674970.1:c.*1546C>T | ENSP00000502493.1:n.*1546C>T | |
| ENST00000675012.1:n.1716C>T | ||
| ENST00000675141.1:c.1673C>T | ENSP00000502420.1:p.Ala558Val | |
| ENST00000675198.1:n.1652C>T | ||
| ENST00000675213.1:c.1727C>T | ENSP00000502218.1:p.Ala576Val | |
| ENST00000675224.1:c.1772C>T | ENSP00000501869.1:p.Ala591Val | |
| ENST00000675253.1:c.*444C>T | ENSP00000502557.1:n.*444C>T | |
| ENST00000675445.1:c.*1444C>T | ENSP00000502253.1:n.*1444C>T | |
| ENST00000675448.1:c.1772C>T | ENSP00000502167.1:p.Ala591Val | |
| ENST00000675521.1:n.1682C>T | ||
| ENST00000675572.1:c.1673C>T | ENSP00000501598.1:p.Ala558Val | |
| ENST00000675641.1:c.*514C>T | ENSP00000501845.1:n.*514C>T | |
| ENST00000675657.1:c.*385C>T | ENSP00000502002.1:n.*385C>T | |
| ENST00000675662.1:n.1567C>T | ||
| ENST00000675789.1:c.1592C>T | ENSP00000501954.1:p.Ala531Val | |
| ENST00000675883.1:c.1691C>T | ENSP00000501592.1:p.Ala564Val | |
| ENST00000675945.1:c.*495C>T | ENSP00000501835.1:n.*495C>T | |
| ENST00000676014.1:c.1715C>T | ENSP00000502058.1:p.Ala572Val | |
| ENST00000676035.1:n.1434C>T | ||
| ENST00000676106.1:n.1809C>T | ||
| ENST00000676137.1:n.1802C>T | ||
| ENST00000676170.1:c.1853C>T | ENSP00000502177.1:p.Ala618Val | |
| ENST00000676318.1:c.*2602C>T | ENSP00000502300.1:n.*2602C>T | |
| ENST00000676336.1:c.*385C>T | ENSP00000502686.1:n.*385C>T | |
| ENST00000676349.1:c.*1460C>T | ENSP00000502155.1:n.*1460C>T | |
| ENST00000676399.1:n.1675C>T | ||
| ENST00000676409.1:n.1832C>T | ||
| ENST00000300417.10:c.1772C>T | ENSP00000300417.6:p.Ala591Val | |
| ENST00000323301.8:c.1772C>T | ENSP00000322937.4:p.Ala591Val | |
| ENST00000373322.1:c.1772C>T | ENSP00000362419.1:p.Ala591Val | |
| ENST00000373324.8:c.1691C>T | ENSP00000362421.4:p.Ala564Val | |
| ENST00000472068.1:n.665C>T | ||
| ENST00000483302.5:n.994C>T | ||
| NM_001005373.3:c.1772C>T | NP_001005373.1:p.Ala591Val | |
| NM_001005374.3:c.1772C>T | NP_001005374.1:p.Ala591Val | |
| NM_001190723.2:c.1691C>T | NP_001177652.1:p.Ala564Val | |
| NM_138361.5:c.1772C>T , LRG_373t1:c.1772C>T | NP_612370.3:p.Ala591Val | |
| XM_006717316.2:c.1673C>T | XP_006717379.1:p.Ala558Val | |
| XM_006717316.4:c.1673C>T | XP_006717379.1:p.Ala558Val | |
| XM_017015283.1:c.1772C>T | XP_016870772.1:p.Ala591Val | |
| XM_017015284.2:c.983C>T | XP_016870773.1:p.Ala328Val | |
| XR_001746415.2:n.2307C>T | ||
| XR_929874.3:n.2131C>T | ||
| NM_001190723.3:c.1691C>T | NP_001177652.1:p.Ala564Val | |
| NM_001005373.4:c.1772C>T MANE Select | NP_001005373.1:p.Ala591Val | |
| NM_001005374.4:c.1772C>T | NP_001005374.1:p.Ala591Val | |
| NM_001384142.1:c.1772C>T | NP_001371071.1:p.Ala591Val | |
| NM_001384143.1:c.1673C>T | NP_001371072.1:p.Ala558Val | |
| NM_001384144.1:c.983C>T | NP_001371073.1:p.Ala328Val | |
| NR_168891.1:n.2301C>T | ||
| NR_168892.1:n.2125C>T |