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
dbSNP Id:
rs2151576634
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2086372C>G , CM000678.2:g.2086372C>G | GRCh38 |
| NC_000016.9:g.2136373C>G , CM000678.1:g.2136373C>G | GRCh37 |
| NC_000016.8:g.2076374C>G | NCBI36 |
| NG_005895.1:g.42067C>G , LRG_487:g.42067C>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*3191C>G | ENSP00000455997.2:n.*3191C>G | |
| ENST00000642206.2:c.4689C>G | ENSP00000495146.2:p.Ile1563Met | |
| ENST00000642365.2:c.4839C>G | ENSP00000495459.2:p.Ile1613Met | |
| ENST00000644417.2:c.*5355C>G | ENSP00000493912.2:n.*5355C>G | |
| ENST00000646464.2:c.*7591C>G | ENSP00000496610.2:n.*7591C>G | |
| ENST00000219476.9:c.4842C>G MANE Select | ENSP00000219476.3:p.Ile1614Met | |
| ENST00000350773.9:c.4773C>G | ENSP00000344383.4:p.Ile1591Met | |
| ENST00000401874.7:c.4641C>G | ENSP00000384468.2:p.Ile1547Met | |
| ENST00000568454.6:c.4674C>G | ENSP00000454487.1:p.Ile1558Met | |
| ENST00000569110.2:c.1065C>G | ||
| ENST00000569930.2:n.2724C>G | ||
| ENST00000642365.1:c.3496C>G | ||
| ENST00000642561.1:c.4713C>G | ENSP00000495099.1:p.Ile1571Met | |
| ENST00000642728.1:n.1024C>G | ||
| ENST00000642791.1:n.439C>G | ||
| ENST00000642797.1:c.4644C>G | ENSP00000493846.1:p.Ile1548Met | |
| ENST00000642936.1:c.4710C>G | ENSP00000494514.1:p.Ile1570Met | |
| ENST00000643088.1:c.4635C>G | ENSP00000494747.1:p.Ile1545Met | |
| ENST00000643177.1:n.856C>G | ||
| ENST00000643426.1:n.2490C>G | ||
| ENST00000643946.1:c.4767C>G | ENSP00000495927.1:p.Ile1589Met | |
| ENST00000644043.1:c.4713C>G | ENSP00000496262.1:p.Ile1571Met | |
| ENST00000644278.1:n.324C>G | ||
| ENST00000644329.1:c.4641C>G | ENSP00000496611.1:p.Ile1547Met | |
| ENST00000644335.1:c.4638C>G | ENSP00000496317.1:p.Ile1546Met | |
| ENST00000644399.1:c.4763C>G | ||
| ENST00000645024.1:n.2926C>G | ||
| ENST00000646388.1:c.4836C>G | ENSP00000495921.1:p.Ile1612Met | |
| ENST00000646557.1:n.3C>G | ||
| ENST00000646634.1:n.3657C>G | ||
| ENST00000646674.1:n.2094C>G | ||
| ENST00000647042.1:n.2065C>G | ||
| ENST00000647180.1:n.1955C>G | ||
| ENST00000219476.7:c.4842C>G | ENSP00000219476.3:p.Ile1614Met | |
| ENST00000350773.8:c.4773C>G | ENSP00000344383.4:p.Ile1591Met | |
| ENST00000382538.10:c.4497C>G | ENSP00000371978.6:p.Ile1499Met | |
| ENST00000401874.6:c.4641C>G | ENSP00000384468.2:p.Ile1547Met | |
| ENST00000439117.6:c.*4009C>G | ENSP00000406980.2:n.*4009C>G | |
| ENST00000439673.6:c.4533C>G | ENSP00000399232.2:p.Ile1511Met | |
| ENST00000497886.5:n.2600C>G | ||
| ENST00000568454.5:c.4674C>G | ENSP00000454487.1:p.Ile1558Met | |
| ENST00000569110.1:c.1024C>G | ||
| ENST00000569930.1:n.1957C>G | ||
| NM_000548.3:c.4842C>G , LRG_487t1:c.4842C>G | NP_000539.2:p.Ile1614Met | |
| NM_001077183.1:c.4641C>G | NP_001070651.1:p.Ile1547Met | |
| NM_001114382.1:c.4773C>G | NP_001107854.1:p.Ile1591Met | |
| XM_005255529.3:c.4713C>G | XP_005255586.2:p.Ile1571Met | |
| XM_005255531.3:c.4644C>G | XP_005255588.2:p.Ile1548Met | |
| XM_011522636.1:c.4896C>G | XP_011520938.1:p.Ile1632Met | |
| XM_011522637.1:c.4893C>G | XP_011520939.1:p.Ile1631Met | |
| XM_011522638.1:c.4785C>G | XP_011520940.1:p.Ile1595Met | |
| XM_011522639.1:c.4767C>G | XP_011520941.1:p.Ile1589Met | |
| XM_011522640.1:c.4764C>G | XP_011520942.1:p.Ile1588Met | |
| XM_011522641.1:c.4533C>G | XP_011520943.1:p.Ile1511Met | |
| NM_000548.4:c.4842C>G | NP_000539.2:p.Ile1614Met | |
| NM_001077183.2:c.4641C>G | NP_001070651.1:p.Ile1547Met | |
| NM_001114382.2:c.4773C>G | NP_001107854.1:p.Ile1591Met | |
| NM_001318827.1:c.4533C>G | NP_001305756.1:p.Ile1511Met | |
| NM_001318829.1:c.4497C>G | NP_001305758.1:p.Ile1499Met | |
| NM_001318831.1:c.4110C>G | NP_001305760.1:p.Ile1370Met | |
| NM_001318832.1:c.4674C>G | NP_001305761.1:p.Ile1558Met | |
| NM_001363528.1:c.4644C>G | NP_001350457.1:p.Ile1548Met | |
| NM_021055.2:c.4713C>G | NP_066399.2:p.Ile1571Met | |
| XM_005255531.4:c.4644C>G | XP_005255588.2:p.Ile1548Met | |
| XM_011522636.2:c.4896C>G | XP_011520938.1:p.Ile1632Met | |
| XM_011522637.2:c.4893C>G | XP_011520939.1:p.Ile1631Met | |
| XM_011522638.2:c.5058C>G | XP_011520940.2:p.Ile1686Met | |
| XM_011522639.2:c.4767C>G | XP_011520941.1:p.Ile1589Met | |
| XM_011522640.2:c.4764C>G | XP_011520942.1:p.Ile1588Met | |
| XM_017023615.1:c.4839C>G | XP_016879104.1:p.Ile1613Met | |
| XM_017023616.1:c.4710C>G | XP_016879105.1:p.Ile1570Met | |
| XM_017023617.1:c.4806C>G | XP_016879106.1:p.Ile1602Met | |
| XM_017023618.1:c.3552C>G | XP_016879107.1:p.Ile1184Met | |
| XM_024450413.1:c.4641C>G | XP_024306181.1:p.Ile1547Met | |
| NM_000548.5:c.4842C>G MANE Select | NP_000539.2:p.Ile1614Met | |
| NM_001370404.1:c.4710C>G | NP_001357333.1:p.Ile1570Met | |
| NM_001370405.1:c.4713C>G | NP_001357334.1:p.Ile1571Met | |
| NM_001077183.3:c.4641C>G | NP_001070651.1:p.Ile1547Met | |
| NM_001114382.3:c.4773C>G | NP_001107854.1:p.Ile1591Met | |
| NM_001318827.2:c.4533C>G | NP_001305756.1:p.Ile1511Met | |
| NM_001318829.2:c.4497C>G | NP_001305758.1:p.Ile1499Met | |
| NM_001318831.2:c.4110C>G | NP_001305760.1:p.Ile1370Met | |
| NM_001318832.2:c.4674C>G | NP_001305761.1:p.Ile1558Met | |
| NM_001363528.2:c.4644C>G | NP_001350457.1:p.Ile1548Met | |
| NM_021055.3:c.4713C>G | NP_066399.2:p.Ile1571Met |