Linked Data
ClinVar Variation Id:
230453
dbSNP Id:
rs755461310
ExAC:
16:2134320 A / C
gnomAD v2:
16-2134320-A-C
gnomAD v4:
16-2084319-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2084319A>C , CM000678.2:g.2084319A>C | GRCh38 |
| NC_000016.9:g.2134320A>C , CM000678.1:g.2134320A>C | GRCh37 |
| NC_000016.8:g.2074321A>C | NCBI36 |
| NG_005895.1:g.40014A>C , LRG_487:g.40014A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2446A>C | ENSP00000455997.2:n.*2446A>C | |
| ENST00000642206.2:c.3944A>C | ENSP00000495146.2:p.Glu1315Ala | |
| ENST00000642365.2:c.4094A>C | ENSP00000495459.2:p.Glu1365Ala | |
| ENST00000644417.2:c.*4477A>C | ENSP00000493912.2:n.*4477A>C | |
| ENST00000646464.2:c.*6846A>C | ENSP00000496610.2:n.*6846A>C | |
| ENST00000219476.9:c.4097A>C MANE Select | ENSP00000219476.3:p.Glu1366Ala | |
| ENST00000350773.9:c.4028A>C | ENSP00000344383.4:p.Glu1343Ala | |
| ENST00000401874.7:c.3896A>C | ENSP00000384468.2:p.Glu1299Ala | |
| ENST00000568454.6:c.3929A>C | ENSP00000454487.1:p.Glu1310Ala | |
| ENST00000569110.2:c.333A>C | ||
| ENST00000569930.2:n.1979A>C | ||
| ENST00000642365.1:c.2751A>C | ||
| ENST00000642561.1:c.3968A>C | ENSP00000495099.1:p.Glu1323Ala | |
| ENST00000642728.1:n.279A>C | ||
| ENST00000642797.1:c.3899A>C | ENSP00000493846.1:p.Glu1300Ala | |
| ENST00000642936.1:c.3965A>C | ENSP00000494514.1:p.Glu1322Ala | |
| ENST00000643088.1:c.3896A>C | ENSP00000494747.1:p.Glu1299Ala | |
| ENST00000643177.1:n.111A>C | ||
| ENST00000643426.1:n.1745A>C | ||
| ENST00000643946.1:c.4028A>C | ENSP00000495927.1:p.Glu1343Ala | |
| ENST00000644043.1:c.3968A>C | ENSP00000496262.1:p.Glu1323Ala | |
| ENST00000644329.1:c.3896A>C | ENSP00000496611.1:p.Glu1299Ala | |
| ENST00000644335.1:c.3899A>C | ENSP00000496317.1:p.Glu1300Ala | |
| ENST00000644399.1:c.4018A>C | ||
| ENST00000645024.1:n.2181A>C | ||
| ENST00000645186.1:c.340A>C | ||
| ENST00000646388.1:c.4097A>C | ENSP00000495921.1:p.Glu1366Ala | |
| ENST00000646634.1:n.2912A>C | ||
| ENST00000646674.1:n.1349A>C | ||
| ENST00000647042.1:n.1320A>C | ||
| ENST00000647180.1:n.1210A>C | ||
| ENST00000219476.7:c.4097A>C | ENSP00000219476.3:p.Glu1366Ala | |
| ENST00000350773.8:c.4028A>C | ENSP00000344383.4:p.Glu1343Ala | |
| ENST00000382538.10:c.3752A>C | ENSP00000371978.6:p.Glu1251Ala | |
| ENST00000401874.6:c.3896A>C | ENSP00000384468.2:p.Glu1299Ala | |
| ENST00000439117.6:c.*3264A>C | ENSP00000406980.2:n.*3264A>C | |
| ENST00000439673.6:c.3788A>C | ENSP00000399232.2:p.Glu1263Ala | |
| ENST00000497886.5:n.1855A>C | ||
| ENST00000568454.5:c.3929A>C | ENSP00000454487.1:p.Glu1310Ala | |
| ENST00000569110.1:c.279A>C | ||
| ENST00000569930.1:n.1212A>C | ||
| NM_000548.3:c.4097A>C , LRG_487t1:c.4097A>C | NP_000539.2:p.Glu1366Ala | |
| NM_001077183.1:c.3896A>C | NP_001070651.1:p.Glu1299Ala | |
| NM_001114382.1:c.4028A>C | NP_001107854.1:p.Glu1343Ala | |
| XM_005255529.3:c.3968A>C | XP_005255586.2:p.Glu1323Ala | |
| XM_005255531.3:c.3899A>C | XP_005255588.2:p.Glu1300Ala | |
| XM_011522636.1:c.4151A>C | XP_011520938.1:p.Glu1384Ala | |
| XM_011522637.1:c.4148A>C | XP_011520939.1:p.Glu1383Ala | |
| XM_011522638.1:c.4040A>C | XP_011520940.1:p.Glu1347Ala | |
| XM_011522639.1:c.4022A>C | XP_011520941.1:p.Glu1341Ala | |
| XM_011522640.1:c.4019A>C | XP_011520942.1:p.Glu1340Ala | |
| XM_011522641.1:c.3788A>C | XP_011520943.1:p.Glu1263Ala | |
| NM_000548.4:c.4097A>C | NP_000539.2:p.Glu1366Ala | |
| NM_001077183.2:c.3896A>C | NP_001070651.1:p.Glu1299Ala | |
| NM_001114382.2:c.4028A>C | NP_001107854.1:p.Glu1343Ala | |
| NM_001318827.1:c.3788A>C | NP_001305756.1:p.Glu1263Ala | |
| NM_001318829.1:c.3752A>C | NP_001305758.1:p.Glu1251Ala | |
| NM_001318831.1:c.3365A>C | NP_001305760.1:p.Glu1122Ala | |
| NM_001318832.1:c.3929A>C | NP_001305761.1:p.Glu1310Ala | |
| NM_001363528.1:c.3899A>C | NP_001350457.1:p.Glu1300Ala | |
| NM_021055.2:c.3968A>C | NP_066399.2:p.Glu1323Ala | |
| XM_005255531.4:c.3899A>C | XP_005255588.2:p.Glu1300Ala | |
| XM_011522636.2:c.4151A>C | XP_011520938.1:p.Glu1384Ala | |
| XM_011522637.2:c.4148A>C | XP_011520939.1:p.Glu1383Ala | |
| XM_011522638.2:c.4313A>C | XP_011520940.2:p.Glu1438Ala | |
| XM_011522639.2:c.4022A>C | XP_011520941.1:p.Glu1341Ala | |
| XM_011522640.2:c.4019A>C | XP_011520942.1:p.Glu1340Ala | |
| XM_017023615.1:c.4094A>C | XP_016879104.1:p.Glu1365Ala | |
| XM_017023616.1:c.3965A>C | XP_016879105.1:p.Glu1322Ala | |
| XM_017023617.1:c.4061A>C | XP_016879106.1:p.Glu1354Ala | |
| XM_017023618.1:c.2807A>C | XP_016879107.1:p.Glu936Ala | |
| XM_024450413.1:c.3896A>C | XP_024306181.1:p.Glu1299Ala | |
| NM_000548.5:c.4097A>C MANE Select | NP_000539.2:p.Glu1366Ala | |
| NM_001370404.1:c.3965A>C | NP_001357333.1:p.Glu1322Ala | |
| NM_001370405.1:c.3968A>C | NP_001357334.1:p.Glu1323Ala | |
| NM_001077183.3:c.3896A>C | NP_001070651.1:p.Glu1299Ala | |
| NM_001114382.3:c.4028A>C | NP_001107854.1:p.Glu1343Ala | |
| NM_001318827.2:c.3788A>C | NP_001305756.1:p.Glu1263Ala | |
| NM_001318829.2:c.3752A>C | NP_001305758.1:p.Glu1251Ala | |
| NM_001318831.2:c.3365A>C | NP_001305760.1:p.Glu1122Ala | |
| NM_001318832.2:c.3929A>C | NP_001305761.1:p.Glu1310Ala | |
| NM_001363528.2:c.3899A>C | NP_001350457.1:p.Glu1300Ala | |
| NM_021055.3:c.3968A>C | NP_066399.2:p.Glu1323Ala |