This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
ClinVar RCV:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2084545dup , CM000678.2:g.2084545dup | GRCh38 |
| NC_000016.9:g.2134546dup , CM000678.1:g.2134546dup | GRCh37 |
| NC_000016.8:g.2074547dup | NCBI36 |
| NG_005895.1:g.40240dup , LRG_487:g.40240dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2672dup | ENSP00000455997.2:n.*2672dup | |
| ENST00000642206.2:c.4170dup | ENSP00000495146.2:p.Glu1391ArgfsTer? | |
| ENST00000642365.2:c.4320dup | ENSP00000495459.2:p.Glu1441ArgfsTer? | |
| ENST00000644417.2:c.*4703dup | ENSP00000493912.2:n.*4703dup | |
| ENST00000646464.2:c.*7072dup | ENSP00000496610.2:n.*7072dup | |
| ENST00000219476.9:c.4323dup MANE Select | ENSP00000219476.3:p.Glu1442ArgfsTer? | |
| ENST00000350773.9:c.4254dup | ENSP00000344383.4:p.Glu1419ArgfsTer? | |
| ENST00000401874.7:c.4122dup | ENSP00000384468.2:p.Glu1375ArgfsTer? | |
| ENST00000568454.6:c.4155dup | ENSP00000454487.1:p.Glu1386ArgfsTer? | |
| ENST00000569110.2:c.559dup | ||
| ENST00000569930.2:n.2205dup | ||
| ENST00000642365.1:c.2977dup | ||
| ENST00000642561.1:c.4194dup | ENSP00000495099.1:p.Glu1399ArgfsTer? | |
| ENST00000642728.1:n.505dup | ||
| ENST00000642797.1:c.4125dup | ENSP00000493846.1:p.Glu1376ArgfsTer? | |
| ENST00000642936.1:c.4191dup | ENSP00000494514.1:p.Glu1398ArgfsTer? | |
| ENST00000643088.1:c.4122dup | ENSP00000494747.1:p.Glu1375ArgfsTer? | |
| ENST00000643177.1:n.337dup | ||
| ENST00000643426.1:n.1971dup | ||
| ENST00000643946.1:c.4254dup | ENSP00000495927.1:p.Glu1419ArgfsTer? | |
| ENST00000644043.1:c.4194dup | ENSP00000496262.1:p.Glu1399ArgfsTer? | |
| ENST00000644329.1:c.4122dup | ENSP00000496611.1:p.Glu1375ArgfsTer? | |
| ENST00000644335.1:c.4125dup | ENSP00000496317.1:p.Glu1376ArgfsTer? | |
| ENST00000644399.1:c.4244dup | ||
| ENST00000645024.1:n.2407dup | ||
| ENST00000646388.1:c.4323dup | ENSP00000495921.1:p.Glu1442ArgfsTer? | |
| ENST00000646634.1:n.3138dup | ||
| ENST00000646674.1:n.1575dup | ||
| ENST00000647042.1:n.1546dup | ||
| ENST00000647180.1:n.1436dup | ||
| ENST00000219476.7:c.4323dup | ENSP00000219476.3:p.Glu1442ArgfsTer? | |
| ENST00000350773.8:c.4254dup | ENSP00000344383.4:p.Glu1419ArgfsTer? | |
| ENST00000382538.10:c.3978dup | ENSP00000371978.6:p.Glu1327ArgfsTer? | |
| ENST00000401874.6:c.4122dup | ENSP00000384468.2:p.Glu1375ArgfsTer? | |
| ENST00000439117.6:c.*3490dup | ENSP00000406980.2:n.*3490dup | |
| ENST00000439673.6:c.4014dup | ENSP00000399232.2:p.Glu1339ArgfsTer? | |
| ENST00000497886.5:n.2081dup | ||
| ENST00000568454.5:c.4155dup | ENSP00000454487.1:p.Glu1386ArgfsTer? | |
| ENST00000569110.1:c.505dup | ||
| ENST00000569930.1:n.1438dup | ||
| NM_000548.3:c.4323dup , LRG_487t1:c.4323dup | NP_000539.2:p.Glu1442ArgfsTer? | |
| NM_001077183.1:c.4122dup | NP_001070651.1:p.Glu1375ArgfsTer? | |
| NM_001114382.1:c.4254dup | NP_001107854.1:p.Glu1419ArgfsTer? | |
| XM_005255529.3:c.4194dup | XP_005255586.2:p.Glu1399ArgfsTer? | |
| XM_005255531.3:c.4125dup | XP_005255588.2:p.Glu1376ArgfsTer? | |
| XM_011522636.1:c.4377dup | XP_011520938.1:p.Glu1460ArgfsTer? | |
| XM_011522637.1:c.4374dup | XP_011520939.1:p.Glu1459ArgfsTer? | |
| XM_011522638.1:c.4266dup | XP_011520940.1:p.Glu1423ArgfsTer? | |
| XM_011522639.1:c.4248dup | XP_011520941.1:p.Glu1417ArgfsTer? | |
| XM_011522640.1:c.4245dup | XP_011520942.1:p.Glu1416ArgfsTer? | |
| XM_011522641.1:c.4014dup | XP_011520943.1:p.Glu1339ArgfsTer? | |
| NM_000548.4:c.4323dup | NP_000539.2:p.Glu1442ArgfsTer? | |
| NM_001077183.2:c.4122dup | NP_001070651.1:p.Glu1375ArgfsTer? | |
| NM_001114382.2:c.4254dup | NP_001107854.1:p.Glu1419ArgfsTer? | |
| NM_001318827.1:c.4014dup | NP_001305756.1:p.Glu1339ArgfsTer? | |
| NM_001318829.1:c.3978dup | NP_001305758.1:p.Glu1327ArgfsTer? | |
| NM_001318831.1:c.3591dup | NP_001305760.1:p.Glu1198ArgfsTer? | |
| NM_001318832.1:c.4155dup | NP_001305761.1:p.Glu1386ArgfsTer? | |
| NM_001363528.1:c.4125dup | NP_001350457.1:p.Glu1376ArgfsTer? | |
| NM_021055.2:c.4194dup | NP_066399.2:p.Glu1399ArgfsTer? | |
| XM_005255531.4:c.4125dup | XP_005255588.2:p.Glu1376ArgfsTer? | |
| XM_011522636.2:c.4377dup | XP_011520938.1:p.Glu1460ArgfsTer? | |
| XM_011522637.2:c.4374dup | XP_011520939.1:p.Glu1459ArgfsTer? | |
| XM_011522638.2:c.4539dup | XP_011520940.2:p.Glu1514ArgfsTer? | |
| XM_011522639.2:c.4248dup | XP_011520941.1:p.Glu1417ArgfsTer? | |
| XM_011522640.2:c.4245dup | XP_011520942.1:p.Glu1416ArgfsTer? | |
| XM_017023615.1:c.4320dup | XP_016879104.1:p.Glu1441ArgfsTer? | |
| XM_017023616.1:c.4191dup | XP_016879105.1:p.Glu1398ArgfsTer? | |
| XM_017023617.1:c.4287dup | XP_016879106.1:p.Glu1430ArgfsTer? | |
| XM_017023618.1:c.3033dup | XP_016879107.1:p.Glu1012ArgfsTer? | |
| XM_024450413.1:c.4122dup | XP_024306181.1:p.Glu1375ArgfsTer? | |
| NM_000548.5:c.4323dup MANE Select | NP_000539.2:p.Glu1442ArgfsTer? | |
| NM_001370404.1:c.4191dup | NP_001357333.1:p.Glu1398ArgfsTer? | |
| NM_001370405.1:c.4194dup | NP_001357334.1:p.Glu1399ArgfsTer? | |
| NM_001077183.3:c.4122dup | NP_001070651.1:p.Glu1375ArgfsTer? | |
| NM_001114382.3:c.4254dup | NP_001107854.1:p.Glu1419ArgfsTer? | |
| NM_001318827.2:c.4014dup | NP_001305756.1:p.Glu1339ArgfsTer? | |
| NM_001318829.2:c.3978dup | NP_001305758.1:p.Glu1327ArgfsTer? | |
| NM_001318831.2:c.3591dup | NP_001305760.1:p.Glu1198ArgfsTer? | |
| NM_001318832.2:c.4155dup | NP_001305761.1:p.Glu1386ArgfsTer? | |
| NM_001363528.2:c.4125dup | NP_001350457.1:p.Glu1376ArgfsTer? | |
| NM_021055.3:c.4194dup | NP_066399.2:p.Glu1399ArgfsTer? |