UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Linked Data
ClinVar Variation Id:
1347802
ClinVar RCV Id:
RCV002044005
dbSNP Id:
rs1555441169
gnomAD v4:
16-2088458-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2088458G>A , CM000678.2:g.2088458G>A | GRCh38 |
| NC_000016.9:g.2138459G>A , CM000678.1:g.2138459G>A | GRCh37 |
| NC_000016.8:g.2078460G>A | NCBI36 |
| NG_005895.1:g.44153G>A , LRG_487:g.44153G>A | |
| NG_008617.1:g.54763C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*3621G>A | ENSP00000455997.2:n.*3621G>A | |
| ENST00000642206.2:c.5119G>A | ENSP00000495146.2:p.Ala1707Thr | |
| ENST00000642365.2:c.5269G>A | ENSP00000495459.2:p.Ala1757Thr | |
| ENST00000644417.2:c.*5785G>A | ENSP00000493912.2:n.*5785G>A | |
| ENST00000646464.2:c.*8021G>A | ENSP00000496610.2:n.*8021G>A | |
| ENST00000219476.9:c.5272G>A MANE Select | ENSP00000219476.3:p.Ala1758Thr | |
| ENST00000350773.9:c.5203G>A | ENSP00000344383.4:p.Ala1735Thr | |
| ENST00000401874.7:c.5071G>A | ENSP00000384468.2:p.Ala1691Thr | |
| ENST00000568454.6:c.5104G>A | ENSP00000454487.1:p.Ala1702Thr | |
| ENST00000569110.2:c.1495G>A | ||
| ENST00000569930.2:n.3154G>A | ||
| ENST00000642365.1:c.3926G>A | ||
| ENST00000642561.1:c.5131G>A | ENSP00000495099.1:p.Ala1711Thr | |
| ENST00000642791.1:n.869G>A | ||
| ENST00000642797.1:c.5074G>A | ENSP00000493846.1:p.Ala1692Thr | |
| ENST00000642936.1:c.5140G>A | ENSP00000494514.1:p.Ala1714Thr | |
| ENST00000643088.1:c.5065G>A | ENSP00000494747.1:p.Ala1689Thr | |
| ENST00000643426.1:n.2920G>A | ||
| ENST00000643946.1:c.5197G>A | ENSP00000495927.1:p.Ala1733Thr | |
| ENST00000644043.1:c.5143G>A | ENSP00000496262.1:p.Ala1715Thr | |
| ENST00000644329.1:c.5158G>A | ENSP00000496611.1:p.Ala1720Thr | |
| ENST00000644335.1:c.5068G>A | ENSP00000496317.1:p.Ala1690Thr | |
| ENST00000644399.1:c.5193G>A | ||
| ENST00000645024.1:n.3356G>A | ||
| ENST00000646388.1:c.5266G>A | ENSP00000495921.1:p.Ala1756Thr | |
| ENST00000646634.1:n.4087G>A | ||
| ENST00000646674.1:n.2524G>A | ||
| ENST00000647042.1:n.2495G>A | ||
| ENST00000647180.1:n.2385G>A | ||
| ENST00000219476.7:c.5272G>A | ENSP00000219476.3:p.Ala1758Thr | |
| ENST00000350773.8:c.5203G>A | ENSP00000344383.4:p.Ala1735Thr | |
| ENST00000382538.10:c.4927G>A | ENSP00000371978.6:p.Ala1643Thr | |
| ENST00000401874.6:c.5071G>A | ENSP00000384468.2:p.Ala1691Thr | |
| ENST00000439117.6:c.*4439G>A | ENSP00000406980.2:n.*4439G>A | |
| ENST00000439673.6:c.4963G>A | ENSP00000399232.2:p.Ala1655Thr | |
| ENST00000497886.5:n.2995G>A | ||
| ENST00000568454.5:c.5104G>A | ENSP00000454487.1:p.Ala1702Thr | |
| ENST00000569110.1:c.1454G>A | ||
| ENST00000569930.1:n.2387G>A | ||
| NM_000548.3:c.5272G>A , LRG_487t1:c.5272G>A | NP_000539.2:p.Ala1758Thr | |
| NM_001077183.1:c.5071G>A | NP_001070651.1:p.Ala1691Thr | |
| NM_001114382.1:c.5203G>A | NP_001107854.1:p.Ala1735Thr | |
| XM_005255529.3:c.5143G>A | XP_005255586.2:p.Ala1715Thr | |
| XM_005255531.3:c.5074G>A | XP_005255588.2:p.Ala1692Thr | |
| XM_011522636.1:c.5326G>A | XP_011520938.1:p.Ala1776Thr | |
| XM_011522637.1:c.5323G>A | XP_011520939.1:p.Ala1775Thr | |
| XM_011522638.1:c.5215G>A | XP_011520940.1:p.Ala1739Thr | |
| XM_011522639.1:c.5197G>A | XP_011520941.1:p.Ala1733Thr | |
| XM_011522640.1:c.5194G>A | XP_011520942.1:p.Ala1732Thr | |
| XM_011522641.1:c.4963G>A | XP_011520943.1:p.Ala1655Thr | |
| NM_000548.4:c.5272G>A | NP_000539.2:p.Ala1758Thr | |
| NM_001077183.2:c.5071G>A | NP_001070651.1:p.Ala1691Thr | |
| NM_001114382.2:c.5203G>A | NP_001107854.1:p.Ala1735Thr | |
| NM_001318827.1:c.4963G>A | NP_001305756.1:p.Ala1655Thr | |
| NM_001318829.1:c.4927G>A | NP_001305758.1:p.Ala1643Thr | |
| NM_001318831.1:c.4540G>A | NP_001305760.1:p.Ala1514Thr | |
| NM_001318832.1:c.5104G>A | NP_001305761.1:p.Ala1702Thr | |
| NM_001363528.1:c.5074G>A | NP_001350457.1:p.Ala1692Thr | |
| NM_021055.2:c.5143G>A | NP_066399.2:p.Ala1715Thr | |
| XM_005255531.4:c.5074G>A | XP_005255588.2:p.Ala1692Thr | |
| XM_011522636.2:c.5326G>A | XP_011520938.1:p.Ala1776Thr | |
| XM_011522637.2:c.5323G>A | XP_011520939.1:p.Ala1775Thr | |
| XM_011522638.2:c.5488G>A | XP_011520940.2:p.Ala1830Thr | |
| XM_011522639.2:c.5197G>A | XP_011520941.1:p.Ala1733Thr | |
| XM_011522640.2:c.5194G>A | XP_011520942.1:p.Ala1732Thr | |
| XM_017023615.1:c.5269G>A | XP_016879104.1:p.Ala1757Thr | |
| XM_017023616.1:c.5140G>A | XP_016879105.1:p.Ala1714Thr | |
| XM_017023617.1:c.5236G>A | XP_016879106.1:p.Ala1746Thr | |
| XM_017023618.1:c.3982G>A | XP_016879107.1:p.Ala1328Thr | |
| XM_024450413.1:c.5158G>A | XP_024306181.1:p.Ala1720Thr | |
| NM_000548.5:c.5272G>A MANE Select | NP_000539.2:p.Ala1758Thr | |
| NM_001370404.1:c.5140G>A | NP_001357333.1:p.Ala1714Thr | |
| NM_001370405.1:c.5131G>A | NP_001357334.1:p.Ala1711Thr | |
| NM_001077183.3:c.5071G>A | NP_001070651.1:p.Ala1691Thr | |
| NM_001114382.3:c.5203G>A | NP_001107854.1:p.Ala1735Thr | |
| NM_001318827.2:c.4963G>A | NP_001305756.1:p.Ala1655Thr | |
| NM_001318829.2:c.4927G>A | NP_001305758.1:p.Ala1643Thr | |
| NM_001318831.2:c.4540G>A | NP_001305760.1:p.Ala1514Thr | |
| NM_001318832.2:c.5104G>A | NP_001305761.1:p.Ala1702Thr | |
| NM_001363528.2:c.5074G>A | NP_001350457.1:p.Ala1692Thr | |
| NM_021055.3:c.5143G>A | NP_066399.2:p.Ala1715Thr |