Linked Data
ClinVar Variation Id:
1116525
dbSNP Id:
rs1567132521
ExAC:
16:2138320 C / T
gnomAD v2:
16-2138320-C-T
gnomAD v4:
16-2088319-C-T
MyVariant Identifiers:
chr16:g.2138320C>T (hg19)
chr16:g.2138320_2138347delinsTCAGCGGGTAGGGAATATGGGGCTCCCT (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2088319C>T , CM000678.2:g.2088319C>T | GRCh38 |
| NC_000016.9:g.2138320C>T , CM000678.1:g.2138320C>T | GRCh37 |
| NC_000016.8:g.2078321C>T | NCBI36 |
| NG_005895.1:g.44014C>T , LRG_487:g.44014C>T | |
| NG_008617.1:g.54902G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*3602C>T | ENSP00000455997.2:n.*3602C>T | |
| ENST00000642206.2:c.5100C>T | ENSP00000495146.2:p.Arg1700= | |
| ENST00000642365.2:c.5250C>T | ENSP00000495459.2:p.Arg1750= | |
| ENST00000644417.2:c.*5766C>T | ENSP00000493912.2:n.*5766C>T | |
| ENST00000646464.2:c.*8002C>T | ENSP00000496610.2:n.*8002C>T | |
| ENST00000219476.9:c.5253C>T MANE Select | ENSP00000219476.3:p.Arg1751= | |
| ENST00000350773.9:c.5184C>T | ENSP00000344383.4:p.Arg1728= | |
| ENST00000401874.7:c.5052C>T | ENSP00000384468.2:p.Arg1684= | |
| ENST00000568454.6:c.5085C>T | ENSP00000454487.1:p.Arg1695= | |
| ENST00000569110.2:c.1476C>T | ||
| ENST00000569930.2:n.3135C>T | ||
| ENST00000642365.1:c.3907C>T | ||
| ENST00000642561.1:c.5112C>T | ENSP00000495099.1:p.Arg1704= | |
| ENST00000642791.1:n.850C>T | ||
| ENST00000642797.1:c.5055C>T | ENSP00000493846.1:p.Arg1685= | |
| ENST00000642936.1:c.5121C>T | ENSP00000494514.1:p.Arg1707= | |
| ENST00000643088.1:c.5046C>T | ENSP00000494747.1:p.Arg1682= | |
| ENST00000643426.1:n.2901C>T | ||
| ENST00000643946.1:c.5178C>T | ENSP00000495927.1:p.Arg1726= | |
| ENST00000644043.1:c.5124C>T | ENSP00000496262.1:p.Arg1708= | |
| ENST00000644329.1:c.5139C>T | ENSP00000496611.1:p.Arg1713= | |
| ENST00000644335.1:c.5049C>T | ENSP00000496317.1:p.Arg1683= | |
| ENST00000644399.1:c.5174C>T | ||
| ENST00000645024.1:n.3337C>T | ||
| ENST00000646388.1:c.5247C>T | ENSP00000495921.1:p.Arg1749= | |
| ENST00000646634.1:n.4068C>T | ||
| ENST00000646674.1:n.2505C>T | ||
| ENST00000647042.1:n.2476C>T | ||
| ENST00000647180.1:n.2366C>T | ||
| ENST00000219476.7:c.5253C>T | ENSP00000219476.3:p.Arg1751= | |
| ENST00000350773.8:c.5184C>T | ENSP00000344383.4:p.Arg1728= | |
| ENST00000382538.10:c.4908C>T | ENSP00000371978.6:p.Arg1636= | |
| ENST00000401874.6:c.5052C>T | ENSP00000384468.2:p.Arg1684= | |
| ENST00000439117.6:c.*4420C>T | ENSP00000406980.2:n.*4420C>T | |
| ENST00000439673.6:c.4944C>T | ENSP00000399232.2:p.Arg1648= | |
| ENST00000497886.5:n.2976C>T | ||
| ENST00000568454.5:c.5085C>T | ENSP00000454487.1:p.Arg1695= | |
| ENST00000569110.1:c.1435C>T | ||
| ENST00000569930.1:n.2368C>T | ||
| NM_000548.3:c.5253C>T , LRG_487t1:c.5253C>T | NP_000539.2:p.Arg1751= | |
| NM_001077183.1:c.5052C>T | NP_001070651.1:p.Arg1684= | |
| NM_001114382.1:c.5184C>T | NP_001107854.1:p.Arg1728= | |
| XM_005255529.3:c.5124C>T | XP_005255586.2:p.Arg1708= | |
| XM_005255531.3:c.5055C>T | XP_005255588.2:p.Arg1685= | |
| XM_011522636.1:c.5307C>T | XP_011520938.1:p.Arg1769= | |
| XM_011522637.1:c.5304C>T | XP_011520939.1:p.Arg1768= | |
| XM_011522638.1:c.5196C>T | XP_011520940.1:p.Arg1732= | |
| XM_011522639.1:c.5178C>T | XP_011520941.1:p.Arg1726= | |
| XM_011522640.1:c.5175C>T | XP_011520942.1:p.Arg1725= | |
| XM_011522641.1:c.4944C>T | XP_011520943.1:p.Arg1648= | |
| NM_000548.4:c.5253C>T | NP_000539.2:p.Arg1751= | |
| NM_001077183.2:c.5052C>T | NP_001070651.1:p.Arg1684= | |
| NM_001114382.2:c.5184C>T | NP_001107854.1:p.Arg1728= | |
| NM_001318827.1:c.4944C>T | NP_001305756.1:p.Arg1648= | |
| NM_001318829.1:c.4908C>T | NP_001305758.1:p.Arg1636= | |
| NM_001318831.1:c.4521C>T | NP_001305760.1:p.Arg1507= | |
| NM_001318832.1:c.5085C>T | NP_001305761.1:p.Arg1695= | |
| NM_001363528.1:c.5055C>T | NP_001350457.1:p.Arg1685= | |
| NM_021055.2:c.5124C>T | NP_066399.2:p.Arg1708= | |
| XM_005255531.4:c.5055C>T | XP_005255588.2:p.Arg1685= | |
| XM_011522636.2:c.5307C>T | XP_011520938.1:p.Arg1769= | |
| XM_011522637.2:c.5304C>T | XP_011520939.1:p.Arg1768= | |
| XM_011522638.2:c.5469C>T | XP_011520940.2:p.Arg1823= | |
| XM_011522639.2:c.5178C>T | XP_011520941.1:p.Arg1726= | |
| XM_011522640.2:c.5175C>T | XP_011520942.1:p.Arg1725= | |
| XM_017023615.1:c.5250C>T | XP_016879104.1:p.Arg1750= | |
| XM_017023616.1:c.5121C>T | XP_016879105.1:p.Arg1707= | |
| XM_017023617.1:c.5217C>T | XP_016879106.1:p.Arg1739= | |
| XM_017023618.1:c.3963C>T | XP_016879107.1:p.Arg1321= | |
| XM_024450413.1:c.5139C>T | XP_024306181.1:p.Arg1713= | |
| NM_000548.5:c.5253C>T MANE Select | NP_000539.2:p.Arg1751= | |
| NM_001370404.1:c.5121C>T | NP_001357333.1:p.Arg1707= | |
| NM_001370405.1:c.5112C>T | NP_001357334.1:p.Arg1704= | |
| NM_001077183.3:c.5052C>T | NP_001070651.1:p.Arg1684= | |
| NM_001114382.3:c.5184C>T | NP_001107854.1:p.Arg1728= | |
| NM_001318827.2:c.4944C>T | NP_001305756.1:p.Arg1648= | |
| NM_001318829.2:c.4908C>T | NP_001305758.1:p.Arg1636= | |
| NM_001318831.2:c.4521C>T | NP_001305760.1:p.Arg1507= | |
| NM_001318832.2:c.5085C>T | NP_001305761.1:p.Arg1695= | |
| NM_001363528.2:c.5055C>T | NP_001350457.1:p.Arg1685= | |
| NM_021055.3:c.5124C>T | NP_066399.2:p.Arg1708= |