Linked Data
ClinVar Variation Id:
1487491
ClinVar RCV Id:
RCV002033563
dbSNP Id:
rs1354941224
gnomAD v4:
18-34851838-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.34851838C>A , CM000680.2:g.34851838C>A | GRCh38 |
| NC_000018.9:g.32431802C>A , CM000680.1:g.32431802C>A | GRCh37 |
| NC_000018.8:g.30685800C>A | NCBI36 |
| NG_009201.1:g.363549C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000283365.14:c.1181C>A | ENSP00000283365.10:p.Pro394His | |
| ENST00000444659.6:c.1442C>A MANE Select | ENSP00000405819.2:p.Pro481His | |
| ENST00000601632.6:c.305C>A | ENSP00000507080.1:p.Pro102His | |
| ENST00000680767.2:c.983C>A | ENSP00000505379.2:p.Pro328His | |
| ENST00000682129.1:c.398C>A | ENSP00000506763.1:p.Pro133His | |
| ENST00000682483.1:c.1181C>A | ENSP00000508159.1:p.Pro394His | |
| ENST00000682581.1:c.905C>A | ENSP00000507924.1:p.Pro302His | |
| ENST00000682923.1:c.905C>A | ENSP00000508131.1:p.Pro302His | |
| ENST00000683370.1:c.1181C>A | ENSP00000507104.1:p.Pro394His | |
| ENST00000683379.1:c.1190C>A | ENSP00000507995.1:p.Pro397His | |
| ENST00000683705.1:c.1181C>A | ENSP00000507911.1:p.Pro394His | |
| ENST00000683876.1:c.227C>A | ENSP00000507423.1:p.Pro76His | |
| ENST00000684228.1:c.227C>A | ENSP00000508278.1:p.Pro76His | |
| ENST00000684266.1:c.1271C>A | ENSP00000507106.1:p.Pro424His | |
| ENST00000684359.1:c.1190C>A | ENSP00000507300.1:p.Pro397His | |
| ENST00000684377.1:c.986C>A | ENSP00000506757.1:p.Pro329His | |
| ENST00000598774.6:c.1190C>A | ENSP00000472031.1:p.Pro397His | |
| ENST00000679372.1:c.*1282C>A | ENSP00000506098.1:n.*1282C>A | |
| ENST00000679678.1:c.488C>A | ENSP00000505120.1:p.Pro163His | |
| ENST00000679796.1:c.1442C>A | ENSP00000506659.1:p.Pro481His | |
| ENST00000679936.1:c.1190C>A | ENSP00000506586.1:p.Pro397His | |
| ENST00000680346.1:c.1190C>A | ENSP00000505947.1:p.Pro397His | |
| ENST00000680767.1:c.1229C>A | ENSP00000505379.1:p.Pro410His | |
| ENST00000680822.1:c.1271C>A | ENSP00000505718.1:p.Pro424His | |
| ENST00000681241.1:c.1181C>A | ENSP00000506495.1:p.Pro394His | |
| ENST00000681274.1:c.896C>A | ENSP00000505183.1:p.Pro299His | |
| ENST00000681470.1:c.1178C>A | ENSP00000505722.1:p.Pro393His | |
| ENST00000681759.1:c.341C>A | ENSP00000506633.1:p.Pro114His | |
| ENST00000269192.11:c.488C>A | ENSP00000269192.7:p.Pro163His | |
| ENST00000283365.13:c.1190C>A | ENSP00000283365.9:p.Pro397His | |
| ENST00000348997.9:c.1352C>A | ENSP00000336682.4:p.Pro451His | |
| ENST00000399113.7:c.1361C>A | ENSP00000382064.3:p.Pro454His | |
| ENST00000399121.9:c.1181C>A | ENSP00000382072.5:p.Pro394His | |
| ENST00000444659.5:c.1361C>A | ENSP00000405819.1:p.Pro454His | |
| ENST00000556414.7:c.317C>A | ENSP00000452255.2:p.Pro106His | |
| ENST00000587723.1:c.158C>A | ENSP00000468262.1:p.Pro53His | |
| ENST00000591182.5:c.305C>A | ENSP00000467720.1:p.Pro102His | |
| ENST00000595022.5:c.1181C>A | ENSP00000473078.1:p.Pro394His | |
| ENST00000596745.5:c.611C>A | ENSP00000469121.1:p.Pro204His | |
| ENST00000597599.5:c.1181C>A | ENSP00000473119.1:p.Pro394His | |
| ENST00000597674.5:c.227C>A | ENSP00000471783.1:p.Pro76His | |
| ENST00000598142.5:c.1190C>A | ENSP00000470716.1:p.Pro397His | |
| ENST00000598334.5:c.1181C>A | ENSP00000470152.1:p.Pro394His | |
| ENST00000598774.5:c.1190C>A | ENSP00000472031.1:p.Pro397His | |
| ENST00000599844.5:c.227C>A | ENSP00000470934.1:p.Pro76His | |
| ENST00000601125.5:c.227C>A | ENSP00000470247.1:p.Pro76His | |
| ENST00000601632.5:n.635C>A | ||
| ENST00000601895.1:n.464C>A | ||
| NM_001198938.1:c.1181C>A | NP_001185867.1:p.Pro394His | |
| NM_001198939.1:c.1181C>A | NP_001185868.1:p.Pro394His | |
| NM_001198940.1:c.1181C>A | NP_001185869.1:p.Pro394His | |
| NM_001198941.1:c.1181C>A | NP_001185870.1:p.Pro394His | |
| NM_001198942.1:c.488C>A | NP_001185871.1:p.Pro163His | |
| NM_001198943.1:c.431C>A | NP_001185872.1:p.Pro144His | |
| NM_001198944.1:c.317C>A | NP_001185873.1:p.Pro106His | |
| NM_001198945.1:c.611C>A | NP_001185874.1:p.Pro204His | |
| NM_001390.4:c.1361C>A | NP_001381.2:p.Pro454His | |
| NM_001391.5:c.1361C>A | NP_001382.2:p.Pro454His | |
| NM_032975.3:c.1190C>A | NP_116757.2:p.Pro397His | |
| NM_032978.6:c.1352C>A | NP_116760.2:p.Pro451His | |
| NM_032979.4:c.1190C>A | NP_116761.2:p.Pro397His | |
| NM_032980.3:c.305C>A | NP_116762.2:p.Pro102His | |
| NM_032981.4:c.227C>A | NP_116763.1:p.Pro76His | |
| XM_005258207.2:c.1442C>A | XP_005258264.1:p.Pro481His | |
| XM_005258212.2:c.1352C>A | XP_005258269.1:p.Pro451His | |
| XM_005258216.3:c.1442C>A | XP_005258273.1:p.Pro481His | |
| XM_005258217.2:c.1271C>A | XP_005258274.1:p.Pro424His | |
| XM_005258218.2:c.1268C>A | XP_005258275.1:p.Pro423His | |
| XM_005258219.3:c.1352C>A | XP_005258276.1:p.Pro451His | |
| XM_005258220.2:c.1181C>A | XP_005258277.1:p.Pro394His | |
| XM_005258221.3:c.1271C>A | XP_005258278.1:p.Pro424His | |
| XM_005258222.3:c.1259C>A | XP_005258279.1:p.Pro420His | |
| XM_005258223.2:c.1352C>A | XP_005258280.1:p.Pro451His | |
| XM_005258224.2:c.488C>A | XP_005258281.1:p.Pro163His | |
| XM_006722395.2:c.1451C>A | XP_006722458.1:p.Pro484His | |
| XM_006722396.2:c.1451C>A | XP_006722459.1:p.Pro484His | |
| XM_006722397.2:c.1451C>A | XP_006722460.1:p.Pro484His | |
| XM_006722398.2:c.1451C>A | XP_006722461.1:p.Pro484His | |
| XM_006722399.2:c.1451C>A | XP_006722462.1:p.Pro484His | |
| XM_006722400.2:c.1361C>A | XP_006722463.1:p.Pro454His | |
| XM_006722401.2:c.1358C>A | XP_006722464.1:p.Pro453His | |
| XM_006722402.2:c.1451C>A | XP_006722465.1:p.Pro484His | |
| XM_006722403.2:c.1451C>A | XP_006722466.1:p.Pro484His | |
| XM_006722404.2:c.1451C>A | XP_006722467.1:p.Pro484His | |
| XM_006722405.2:c.1280C>A | XP_006722468.1:p.Pro427His | |
| XM_006722406.1:c.1361C>A | XP_006722469.1:p.Pro454His | |
| XM_006722407.2:c.1190C>A | XP_006722470.1:p.Pro397His | |
| XM_006722408.2:c.1190C>A | XP_006722471.1:p.Pro397His | |
| XM_006722409.1:c.1361C>A | XP_006722472.1:p.Pro454His | |
| XM_006722410.2:c.1190C>A | XP_006722473.1:p.Pro397His | |
| XM_006722411.2:c.497C>A | XP_006722474.1:p.Pro166His | |
| XM_006722412.2:c.317C>A | XP_006722475.1:p.Pro106His | |
| XM_006722413.2:c.227C>A | XP_006722476.1:p.Pro76His | |
| XM_006722414.2:c.224C>A | XP_006722477.1:p.Pro75His | |
| XM_011525851.1:c.1451C>A | XP_011524153.1:p.Pro484His | |
| XM_011525852.1:c.1448C>A | XP_011524154.1:p.Pro483His | |
| XM_011525853.1:c.1181C>A | XP_011524155.1:p.Pro394His | |
| XM_005258221.5:c.1271C>A | XP_005258278.1:p.Pro424His | |
| XM_011525853.3:c.1181C>A | XP_011524155.1:p.Pro394His | |
| XM_017025575.2:c.1271C>A | XP_016881064.1:p.Pro424His | |
| XM_017025576.2:c.1190C>A | XP_016881065.1:p.Pro397His | |
| XM_017025577.2:c.1181C>A | XP_016881066.1:p.Pro394His | |
| XM_017025578.2:c.1271C>A | XP_016881067.1:p.Pro424His | |
| XM_017025579.2:c.1271C>A | XP_016881068.1:p.Pro424His | |
| XM_017025580.1:c.1271C>A | XP_016881069.1:p.Pro424His | |
| XM_017025581.2:c.1271C>A | XP_016881070.1:p.Pro424His | |
| XM_017025582.2:c.1271C>A | XP_016881071.1:p.Pro424His | |
| XM_017025584.2:c.1190C>A | XP_016881073.1:p.Pro397His | |
| XM_017025585.2:c.1187C>A | XP_016881074.1:p.Pro396His | |
| XM_017025586.2:c.1187C>A | XP_016881075.1:p.Pro396His | |
| XM_017025587.2:c.1181C>A | XP_016881076.1:p.Pro394His | |
| XM_017025588.2:c.1181C>A | XP_016881077.1:p.Pro394His | |
| XM_017025589.2:c.1181C>A | XP_016881078.1:p.Pro394His | |
| XM_017025590.2:c.1181C>A | XP_016881079.1:p.Pro394His | |
| XM_017025591.2:c.1181C>A | XP_016881080.1:p.Pro394His | |
| XM_017025593.2:c.1178C>A | XP_016881082.1:p.Pro393His | |
| XM_017025594.2:c.1178C>A | XP_016881083.1:p.Pro393His | |
| XM_017025595.1:c.1271C>A | XP_016881084.1:p.Pro424His | |
| XM_017025597.2:c.1178C>A | XP_016881086.1:p.Pro393His | |
| XM_017025598.2:c.1178C>A | XP_016881087.1:p.Pro393His | |
| XM_017025599.2:c.227C>A | XP_016881088.1:p.Pro76His | |
| XM_024451096.1:c.1178C>A | XP_024306864.1:p.Pro393His | |
| XM_024451097.1:c.1268C>A | XP_024306865.1:p.Pro423His | |
| XM_024451098.1:c.1181C>A | XP_024306866.1:p.Pro394His | |
| XR_001753152.1:n.1844C>A | ||
| XR_001753153.1:n.1844C>A | ||
| XR_001753154.1:n.1934C>A | ||
| XR_001753155.1:n.1844C>A | ||
| XR_001753156.1:n.1934C>A | ||
| XR_001753157.1:n.1841C>A | ||
| XR_001753158.1:n.1844C>A | ||
| XR_001753159.1:n.1931C>A | ||
| XR_001753160.1:n.1841C>A | ||
| XR_001753161.1:n.1931C>A | ||
| XR_001753162.1:n.1934C>A | ||
| XR_001753163.1:n.1841C>A | ||
| XR_002958166.1:n.1451C>A | ||
| NM_001198938.2:c.1181C>A | NP_001185867.1:p.Pro394His | |
| NM_001198939.2:c.1181C>A | NP_001185868.1:p.Pro394His | |
| NM_001198940.2:c.1181C>A | NP_001185869.1:p.Pro394His | |
| NM_001198941.2:c.1181C>A | NP_001185870.1:p.Pro394His | |
| NM_001198945.2:c.611C>A | NP_001185874.1:p.Pro204His | |
| NM_032978.7:c.1352C>A | NP_116760.2:p.Pro451His | |
| NM_032979.5:c.1190C>A | NP_116761.2:p.Pro397His | |
| NM_032980.4:c.305C>A | NP_116762.2:p.Pro102His | |
| NM_032981.5:c.227C>A | NP_116763.1:p.Pro76His | |
| NM_001386753.1:c.1181C>A | NP_001373682.1:p.Pro394His | |
| NM_001386754.1:c.1271C>A | NP_001373683.1:p.Pro424His | |
| NM_001386755.1:c.1271C>A | NP_001373684.1:p.Pro424His | |
| NM_001386756.1:c.1271C>A | NP_001373685.1:p.Pro424His | |
| NM_001386757.1:c.1271C>A | NP_001373686.1:p.Pro424His | |
| NM_001386758.1:c.1271C>A | NP_001373687.1:p.Pro424His | |
| NM_001386759.1:c.1271C>A | NP_001373688.1:p.Pro424His | |
| NM_001386760.1:c.1268C>A | NP_001373689.1:p.Pro423His | |
| NM_001386761.1:c.1190C>A | NP_001373690.1:p.Pro397His | |
| NM_001386762.1:c.1187C>A | NP_001373691.1:p.Pro396His | |
| NM_001386763.1:c.1181C>A | NP_001373692.1:p.Pro394His | |
| NM_001386764.1:c.1181C>A | NP_001373693.1:p.Pro394His | |
| NM_001386765.1:c.1181C>A | NP_001373694.1:p.Pro394His | |
| NM_001386766.1:c.1181C>A | NP_001373695.1:p.Pro394His | |
| NM_001386767.1:c.1181C>A | NP_001373696.1:p.Pro394His | |
| NM_001386768.1:c.1178C>A | NP_001373697.1:p.Pro393His | |
| NM_001386769.1:c.1178C>A | NP_001373698.1:p.Pro393His | |
| NM_001386770.1:c.1271C>A | NP_001373699.1:p.Pro424His | |
| NM_001386771.1:c.1181C>A | NP_001373700.1:p.Pro394His | |
| NM_001386772.1:c.1181C>A | NP_001373701.1:p.Pro394His | |
| NM_001386773.1:c.1178C>A | NP_001373702.1:p.Pro393His | |
| NM_001386774.1:c.1178C>A | NP_001373703.1:p.Pro393His | |
| NM_001386788.1:c.1442C>A | NP_001373717.1:p.Pro481His | |
| NM_001386795.1:c.1442C>A MANE Select | NP_001373724.1:p.Pro481His | |
| NM_001390.5:c.1361C>A | NP_001381.2:p.Pro454His | |
| NM_032975.4:c.1190C>A | NP_116757.2:p.Pro397His |