Linked Data
ClinVar Variation Id:
238218
dbSNP Id:
rs201866563
ExAC:
3:9982648 G / A
gnomAD v2:
3-9982648-G-A
gnomAD v3:
3-9940964-G-A
gnomAD v4:
3-9940964-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.9940964G>A , CM000665.2:g.9940964G>A | GRCh38 |
| NC_000003.11:g.9982648G>A , CM000665.1:g.9982648G>A | GRCh37 |
| NC_000003.10:g.9957648G>A | NCBI36 |
| NG_017069.1:g.12124G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696835.1:c.*1223G>A | ENSP00000512913.1:n.*1223G>A | |
| ENST00000696836.1:c.*1223G>A | ENSP00000512914.1:n.*1223G>A | |
| ENST00000696837.1:c.*2052G>A | ENSP00000512915.1:n.*2052G>A | |
| ENST00000696838.1:c.*1223G>A | ENSP00000512916.1:n.*1223G>A | |
| ENST00000696839.1:c.*1223G>A | ENSP00000512917.1:n.*1223G>A | |
| ENST00000707135.1:n.1221-330C>T (PRRT3) | ||
| ENST00000707136.1:n.1826-336C>T (PRRT3) | ||
| ENST00000397170.8:c.575G>A (CRELD1) | ENSP00000380355.4:p.Cys192Tyr | |
| ENST00000414117.6:c.464G>A (CRELD1) | ENSP00000411021.2:p.Cys155Tyr | |
| ENST00000467713.6:n.681G>A (CRELD1) | ||
| ENST00000489674.6:n.151G>A (CRELD1) | ||
| ENST00000673635.2:c.*241G>A (CRELD1) | ENSP00000501186.2:n.*241G>A | |
| ENST00000673677.2:c.575G>A (CRELD1) | ENSP00000500985.2:p.Cys192Tyr | |
| ENST00000673737.2:c.575G>A (CRELD1) | ENSP00000501208.1:p.Cys192Tyr | |
| ENST00000673935.2:c.575G>A (CRELD1) | ENSP00000500961.2:p.Cys192Tyr | |
| ENST00000674067.2:c.*157G>A (CRELD1) | ENSP00000501009.2:n.*157G>A | |
| ENST00000681970.1:n.1241G>A | ||
| ENST00000682120.1:n.677G>A (CRELD1) | ||
| ENST00000682122.1:c.*223G>A | ENSP00000507036.1:n.*223G>A | |
| ENST00000682200.1:c.*66G>A (CRELD1) | ENSP00000508321.1:n.*66G>A | |
| ENST00000682318.1:c.*66G>A (CRELD1) | ENSP00000507946.1:n.*66G>A | |
| ENST00000682397.1:c.*66G>A (CRELD1) | ENSP00000507177.1:n.*66G>A | |
| ENST00000682403.1:c.*66G>A (CRELD1) | ENSP00000507865.1:n.*66G>A | |
| ENST00000682570.1:c.575G>A (CRELD1) | ENSP00000507973.1:p.Cys192Tyr | |
| ENST00000682642.1:c.575G>A (CRELD1) | ENSP00000507251.1:p.Cys192Tyr | |
| ENST00000682771.1:c.575G>A (CRELD1) | ENSP00000507114.1:p.Cys192Tyr | |
| ENST00000682783.1:c.575G>A (CRELD1) | ENSP00000508358.1:p.Cys192Tyr | |
| ENST00000682790.1:c.*149G>A (CRELD1) | ENSP00000507904.1:n.*149G>A | |
| ENST00000682798.1:n.1180G>A (CRELD1) | ||
| ENST00000682866.1:n.594G>A (CRELD1) | ||
| ENST00000682884.1:n.1069G>A (CRELD1) | ||
| ENST00000682906.1:c.*66G>A (CRELD1) | ENSP00000507674.1:n.*66G>A | |
| ENST00000682907.1:c.575G>A (CRELD1) | ENSP00000508209.1:p.Cys192Tyr | |
| ENST00000682929.1:c.575G>A (CRELD1) | ENSP00000507930.1:p.Cys192Tyr | |
| ENST00000683061.1:n.2158G>A | ||
| ENST00000683083.1:n.683G>A (CRELD1) | ||
| ENST00000683127.1:c.575G>A (CRELD1) | ENSP00000506906.1:p.Cys192Tyr | |
| ENST00000683189.1:c.575G>A (CRELD1) | ENSP00000508018.1:p.Cys192Tyr | |
| ENST00000683232.1:c.*66G>A (CRELD1) | ENSP00000506842.1:n.*66G>A | |
| ENST00000683239.1:n.705G>A (CRELD1) | ||
| ENST00000683279.1:n.654G>A (CRELD1) | ||
| ENST00000683301.1:c.*66G>A (CRELD1) | ENSP00000507718.1:n.*66G>A | |
| ENST00000683316.1:c.575G>A (CRELD1) | ENSP00000507076.1:p.Cys192Tyr | |
| ENST00000683388.1:n.2679G>A (CRELD1) | ||
| ENST00000683467.1:n.797G>A (CRELD1) | ||
| ENST00000683484.1:c.*223G>A | ENSP00000507040.1:n.*223G>A | |
| ENST00000683547.1:c.575G>A (CRELD1) | ENSP00000507258.1:p.Cys192Tyr | |
| ENST00000683601.1:c.575G>A (CRELD1) | ENSP00000507737.1:p.Cys192Tyr | |
| ENST00000683603.1:c.575G>A (CRELD1) | ENSP00000508016.1:p.Cys192Tyr | |
| ENST00000683736.1:c.350-147G>A (CRELD1) | ENSP00000507761.1:n.350-147G>A | |
| ENST00000683835.1:c.575G>A (CRELD1) | ENSP00000508148.1:p.Cys192Tyr | |
| ENST00000683849.1:c.*66G>A (CRELD1) | ENSP00000506901.1:n.*66G>A | |
| ENST00000683888.1:n.1180G>A (CRELD1) | ||
| ENST00000683891.1:c.*66G>A (CRELD1) | ENSP00000506972.1:n.*66G>A | |
| ENST00000683921.1:c.*629G>A (CRELD1) | ENSP00000507395.1:n.*629G>A | |
| ENST00000683970.1:c.575G>A (CRELD1) | ENSP00000507906.1:p.Cys192Tyr | |
| ENST00000683982.1:c.575G>A (CRELD1) | ENSP00000507437.1:p.Cys192Tyr | |
| ENST00000684181.1:c.575G>A (CRELD1) | ENSP00000507522.1:p.Cys192Tyr | |
| ENST00000684212.1:c.575G>A (CRELD1) | ENSP00000507565.1:p.Cys192Tyr | |
| ENST00000684243.1:c.*241G>A (CRELD1) | ENSP00000506959.1:n.*241G>A | |
| ENST00000684291.1:c.575G>A (CRELD1) | ENSP00000506927.1:p.Cys192Tyr | |
| ENST00000684318.1:c.575G>A (CRELD1) | ENSP00000508180.1:p.Cys192Tyr | |
| ENST00000684419.1:n.1157G>A (CRELD1) | ||
| ENST00000684493.1:c.575G>A (CRELD1) | ENSP00000507127.1:p.Cys192Tyr | |
| ENST00000684526.1:c.*66G>A (CRELD1) | ENSP00000508163.1:n.*66G>A | |
| ENST00000684532.1:c.575G>A (CRELD1) | ENSP00000508212.1:p.Cys192Tyr | |
| ENST00000684601.1:c.575G>A (CRELD1) | ENSP00000507886.1:p.Cys192Tyr | |
| ENST00000684613.1:c.575G>A (CRELD1) | ENSP00000508218.1:p.Cys192Tyr | |
| ENST00000684629.1:c.*66G>A (CRELD1) | ENSP00000506879.1:n.*66G>A | |
| ENST00000684648.1:c.*66G>A (CRELD1) | ENSP00000507931.1:n.*66G>A | |
| ENST00000383811.8:c.575G>A (CRELD1) | ENSP00000373322.3:p.Cys192Tyr | |
| ENST00000452070.6:c.575G>A (CRELD1) MANE Select | ENSP00000393643.2:p.Cys192Tyr | |
| ENST00000673635.1:c.430G>A (CRELD1) | ENSP00000501186.1:n.430G>A | |
| ENST00000673677.1:c.845G>A | ENSP00000500985.1:n.845G>A | |
| ENST00000673737.1:c.575G>A (CRELD1) | ENSP00000501208.1:p.Cys192Tyr | |
| ENST00000673935.1:c.102G>A (CRELD1) | ||
| ENST00000674057.1:c.*241G>A (CRELD1) | ENSP00000501128.1:n.*241G>A | |
| ENST00000674067.1:c.340G>A | ENSP00000501009.1:n.340G>A | |
| ENST00000326434.9:c.575G>A (CRELD1) | ENSP00000321856.5:p.Cys192Tyr | |
| ENST00000383811.7:c.575G>A (CRELD1) | ENSP00000373322.3:p.Cys192Tyr | |
| ENST00000397170.7:c.575G>A (CRELD1) | ENSP00000380355.3:p.Cys192Tyr | |
| ENST00000414117.5:c.*66G>A (CRELD1) | ENSP00000411021.1:n.*66G>A | |
| ENST00000452070.5:c.575G>A (CRELD1) | ENSP00000393643.1:p.Cys192Tyr | |
| NM_001031717.3:c.575G>A (CRELD1) | NP_001026887.1:p.Cys192Tyr | |
| NM_001077415.2:c.575G>A (CRELD1) | NP_001070883.1:p.Cys192Tyr | |
| NM_015513.4:c.575G>A (CRELD1) | NP_056328.2:p.Cys192Tyr | |
| XM_011534108.1:c.575G>A (CRELD1) | XP_011532410.1:p.Cys192Tyr | |
| XR_002959584.1:n.659G>A (CRELD1) | ||
| NM_001031717.4:c.575G>A (CRELD1) | NP_001026887.2:p.Cys192Tyr | |
| NM_001077415.3:c.575G>A (CRELD1) MANE Select | NP_001070883.2:p.Cys192Tyr | |
| NM_001374316.1:c.575G>A (CRELD1) | NP_001361245.1:p.Cys192Tyr | |
| NM_001374317.1:c.575G>A (CRELD1) | NP_001361246.1:p.Cys192Tyr | |
| NM_001374318.1:c.575G>A (CRELD1) | NP_001361247.1:p.Cys192Tyr | |
| NM_001374319.1:c.575G>A (CRELD1) | NP_001361248.1:p.Cys192Tyr | |
| NM_001374320.1:c.575G>A (CRELD1) | NP_001361249.1:p.Cys192Tyr | |
| NM_015513.6:c.575G>A (CRELD1) | NP_056328.3:p.Cys192Tyr | |
| NR_164475.1:n.613G>A (CRELD1) | ||
| NR_164476.1:n.589G>A (CRELD1) | ||
| NR_164477.1:n.963G>A (CRELD1) |