Linked Data
ClinVar Variation Id:
467858
dbSNP Id:
rs774727624
ExAC:
16:2112526 A / G
gnomAD v2:
16-2112526-A-G
gnomAD v3:
16-2062525-A-G
gnomAD v4:
16-2062525-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2062525A>G , CM000678.2:g.2062525A>G | GRCh38 |
| NC_000016.9:g.2112526A>G , CM000678.1:g.2112526A>G | GRCh37 |
| NC_000016.8:g.2052527A>G | NCBI36 |
| NG_005895.1:g.18220A>G , LRG_487:g.18220A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.1286A>G | ENSP00000455997.2:p.Tyr429Cys | |
| ENST00000642206.2:c.1331A>G | ENSP00000495146.2:p.Tyr444Cys | |
| ENST00000642365.2:c.1286A>G | ENSP00000495459.2:p.Tyr429Cys | |
| ENST00000644417.2:c.*723A>G | ENSP00000493912.2:n.*723A>G | |
| ENST00000646464.2:c.*891A>G | ENSP00000496610.2:n.*891A>G | |
| ENST00000219476.9:c.1286A>G MANE Select | ENSP00000219476.3:p.Tyr429Cys | |
| ENST00000350773.9:c.1286A>G | ENSP00000344383.4:p.Tyr429Cys | |
| ENST00000401874.7:c.1286A>G | ENSP00000384468.2:p.Tyr429Cys | |
| ENST00000463601.2:n.196A>G | ||
| ENST00000467949.2:n.456A>G | ||
| ENST00000568454.6:c.1319A>G | ENSP00000454487.1:p.Tyr440Cys | |
| ENST00000642561.1:c.1286A>G | ENSP00000495099.1:p.Tyr429Cys | |
| ENST00000642797.1:c.1286A>G | ENSP00000493846.1:p.Tyr429Cys | |
| ENST00000642812.1:n.1331A>G | ||
| ENST00000642936.1:c.1286A>G | ENSP00000494514.1:p.Tyr429Cys | |
| ENST00000643088.1:c.1286A>G | ENSP00000494747.1:p.Tyr429Cys | |
| ENST00000643149.1:n.3296A>G | ||
| ENST00000643298.1:c.*788A>G | ENSP00000494393.1:n.*788A>G | |
| ENST00000643745.1:c.*218A>G | ENSP00000495948.1:n.*218A>G | |
| ENST00000643946.1:c.1286A>G | ENSP00000495927.1:p.Tyr429Cys | |
| ENST00000644043.1:c.1286A>G | ENSP00000496262.1:p.Tyr429Cys | |
| ENST00000644135.1:c.1286A>G | ENSP00000495644.1:p.Tyr429Cys | |
| ENST00000644222.1:n.1373A>G | ||
| ENST00000644329.1:c.1286A>G | ENSP00000496611.1:p.Tyr429Cys | |
| ENST00000644335.1:c.1286A>G | ENSP00000496317.1:p.Tyr429Cys | |
| ENST00000644399.1:c.1279A>G | ||
| ENST00000644665.1:n.2460A>G | ||
| ENST00000644847.1:n.278A>G | ||
| ENST00000645591.1:n.2344A>G | ||
| ENST00000646388.1:c.1286A>G | ENSP00000495921.1:p.Tyr429Cys | |
| ENST00000646634.1:n.299A>G | ||
| ENST00000647234.1:n.3044A>G | ||
| ENST00000647242.1:n.1926-4A>G | ||
| ENST00000219476.7:c.1286A>G | ENSP00000219476.3:p.Tyr429Cys | |
| ENST00000350773.8:c.1286A>G | ENSP00000344383.4:p.Tyr429Cys | |
| ENST00000382538.10:c.1139A>G | ENSP00000371978.6:p.Tyr380Cys | |
| ENST00000401874.6:c.1286A>G | ENSP00000384468.2:p.Tyr429Cys | |
| ENST00000439117.6:c.*585A>G | ENSP00000406980.2:n.*585A>G | |
| ENST00000439673.6:c.1175A>G | ENSP00000399232.2:p.Tyr392Cys | |
| ENST00000463601.1:n.449A>G | ||
| ENST00000467949.1:c.440A>G | ENSP00000454997.1:p.Tyr147Cys | |
| ENST00000568454.5:c.1319A>G | ENSP00000454487.1:p.Tyr440Cys | |
| ENST00000568566.5:c.8A>G | ENSP00000455997.1:p.Tyr3Cys | |
| NM_000548.3:c.1286A>G , LRG_487t1:c.1286A>G | NP_000539.2:p.Tyr429Cys | |
| NM_001077183.1:c.1286A>G | NP_001070651.1:p.Tyr429Cys | |
| NM_001114382.1:c.1286A>G | NP_001107854.1:p.Tyr429Cys | |
| XM_005255529.3:c.1286A>G | XP_005255586.2:p.Tyr429Cys | |
| XM_005255531.3:c.1286A>G | XP_005255588.2:p.Tyr429Cys | |
| XM_011522636.1:c.1286A>G | XP_011520938.1:p.Tyr429Cys | |
| XM_011522637.1:c.1286A>G | XP_011520939.1:p.Tyr429Cys | |
| XM_011522638.1:c.1175A>G | XP_011520940.1:p.Tyr392Cys | |
| XM_011522639.1:c.1286A>G | XP_011520941.1:p.Tyr429Cys | |
| XM_011522640.1:c.1286A>G | XP_011520942.1:p.Tyr429Cys | |
| XM_011522641.1:c.1175A>G | XP_011520943.1:p.Tyr392Cys | |
| NM_000548.4:c.1286A>G | NP_000539.2:p.Tyr429Cys | |
| NM_001077183.2:c.1286A>G | NP_001070651.1:p.Tyr429Cys | |
| NM_001114382.2:c.1286A>G | NP_001107854.1:p.Tyr429Cys | |
| NM_001318827.1:c.1175A>G | NP_001305756.1:p.Tyr392Cys | |
| NM_001318829.1:c.1139A>G | NP_001305758.1:p.Tyr380Cys | |
| NM_001318831.1:c.686A>G | NP_001305760.1:p.Tyr229Cys | |
| NM_001318832.1:c.1319A>G | NP_001305761.1:p.Tyr440Cys | |
| NM_001363528.1:c.1286A>G | NP_001350457.1:p.Tyr429Cys | |
| NM_021055.2:c.1286A>G | NP_066399.2:p.Tyr429Cys | |
| XM_005255531.4:c.1286A>G | XP_005255588.2:p.Tyr429Cys | |
| XM_011522636.2:c.1286A>G | XP_011520938.1:p.Tyr429Cys | |
| XM_011522637.2:c.1286A>G | XP_011520939.1:p.Tyr429Cys | |
| XM_011522638.2:c.1448A>G | XP_011520940.2:p.Tyr483Cys | |
| XM_011522639.2:c.1286A>G | XP_011520941.1:p.Tyr429Cys | |
| XM_011522640.2:c.1286A>G | XP_011520942.1:p.Tyr429Cys | |
| XM_017023615.1:c.1286A>G | XP_016879104.1:p.Tyr429Cys | |
| XM_017023616.1:c.1286A>G | XP_016879105.1:p.Tyr429Cys | |
| XM_017023617.1:c.1448A>G | XP_016879106.1:p.Tyr483Cys | |
| XM_017023618.1:c.-59A>G | XP_016879107.1:n.-59A>G | |
| XM_024450413.1:c.1286A>G | XP_024306181.1:p.Tyr429Cys | |
| NM_000548.5:c.1286A>G MANE Select | NP_000539.2:p.Tyr429Cys | |
| NM_001370404.1:c.1286A>G | NP_001357333.1:p.Tyr429Cys | |
| NM_001370405.1:c.1286A>G | NP_001357334.1:p.Tyr429Cys | |
| NM_001077183.3:c.1286A>G | NP_001070651.1:p.Tyr429Cys | |
| NM_001114382.3:c.1286A>G | NP_001107854.1:p.Tyr429Cys | |
| NM_001318827.2:c.1175A>G | NP_001305756.1:p.Tyr392Cys | |
| NM_001318829.2:c.1139A>G | NP_001305758.1:p.Tyr380Cys | |
| NM_001318831.2:c.686A>G | NP_001305760.1:p.Tyr229Cys | |
| NM_001318832.2:c.1319A>G | NP_001305761.1:p.Tyr440Cys | |
| NM_001363528.2:c.1286A>G | NP_001350457.1:p.Tyr429Cys | |
| NM_021055.3:c.1286A>G | NP_066399.2:p.Tyr429Cys |