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.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.11023571G= , CM000681.2:g.11023571G= | GRCh38 |
| NC_000019.9:g.11134247G= , CM000681.1:g.11134247G= | GRCh37 |
| NC_000019.8:g.10995247G= | NCBI36 |
| NG_011556.2:g.67650G= | |
| NG_011556.3:g.67640G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000711079.1:c.2913G= | ENSP00000518564.1:p.Val971= | |
| ENST00000704344.1:c.2913G= | ENSP00000515855.1:p.Val971= | |
| ENST00000704345.1:c.2904G= | ENSP00000515856.1:p.Val968= | |
| ENST00000646693.2:c.2913G= MANE Plus Clinical | ENSP00000495368.1:p.Val971= | |
| ENST00000344626.10:c.2913G= MANE Select | ENSP00000343896.4:p.Val971= | |
| ENST00000429416.8:c.2913G= | ENSP00000395654.1:p.Val971= | |
| ENST00000444061.8:c.2913G= | ENSP00000392837.2:p.Val971= | |
| ENST00000590574.6:c.2913G= | ENSP00000466963.1:p.Val971= | |
| ENST00000591545.6:c.2786G= | ||
| ENST00000592604.6:n.1244G= | ||
| ENST00000642350.1:c.1398G= | ENSP00000495355.1:p.Val466= | |
| ENST00000642508.1:c.274G= | ||
| ENST00000642628.1:c.2913G= | ENSP00000496498.1:p.Val971= | |
| ENST00000642726.1:c.2913G= | ENSP00000494353.1:p.Val971= | |
| ENST00000643208.1:c.1470G= | ENSP00000496074.1:p.Val490= | |
| ENST00000643296.1:c.2913G= | ENSP00000496635.1:p.Val971= | |
| ENST00000643534.1:c.1198G= | ||
| ENST00000643549.1:c.2913G= | ENSP00000493975.1:p.Val971= | |
| ENST00000643857.1:c.1268G= | ||
| ENST00000643995.1:c.2327G= | ||
| ENST00000644065.1:c.1640G= | ||
| ENST00000644267.1:n.1268G= | ||
| ENST00000644290.1:c.1170G= | ||
| ENST00000644327.1:c.1684G= | ||
| ENST00000644737.1:c.2913G= | ENSP00000495548.1:p.Val971= | |
| ENST00000644963.1:c.1558G= | ||
| ENST00000645061.1:c.1401G= | ENSP00000493690.1:p.Val467= | |
| ENST00000645460.1:c.2913G= | ENSP00000494463.1:p.Val971= | |
| ENST00000645648.1:c.777G= | ENSP00000493521.1:p.Val259= | |
| ENST00000646183.1:c.1259G= | ||
| ENST00000646236.1:c.396G= | ENSP00000493925.1:p.Val132= | |
| ENST00000646484.1:c.2913G= | ENSP00000495536.1:p.Val971= | |
| ENST00000646510.1:c.2913G= | ENSP00000494772.1:p.Val971= | |
| ENST00000646513.1:c.747G= | ENSP00000495457.1:p.Val249= | |
| ENST00000646593.1:c.761G= | ENSP00000494341.1:n.761G= | |
| ENST00000646693.1:c.2913G= | ENSP00000495368.1:p.Val971= | |
| ENST00000646746.1:c.1213G= | ||
| ENST00000647230.1:c.2913G= | ENSP00000494676.1:p.Val971= | |
| ENST00000647268.1:c.1266G= | ENSP00000496176.1:p.Val422= | |
| ENST00000344626.8:c.2913G= | ENSP00000343896.4:p.Val971= | |
| ENST00000413806.7:c.3105G= | ENSP00000414727.3:p.Val1035= | |
| ENST00000429416.7:c.2913G= | ENSP00000395654.1:p.Val971= | |
| ENST00000444061.7:c.2913G= | ENSP00000392837.2:p.Val971= | |
| ENST00000450717.7:c.2913G= | ENSP00000397783.3:p.Val971= | |
| ENST00000541122.6:c.2913G= | ENSP00000445036.2:p.Val971= | |
| ENST00000585799.5:n.1441G= | ||
| ENST00000586122.5:n.495G= | ||
| ENST00000589677.5:c.2913G= | ENSP00000464778.1:p.Val971= | |
| ENST00000590574.5:c.2913G= | ENSP00000466963.1:p.Val971= | |
| ENST00000591545.5:n.2787G= | ||
| ENST00000591595.5:n.985G= | ||
| ENST00000592604.5:n.826G= | ||
| NM_001128844.1:c.2913G= | NP_001122316.1:p.Val971= | |
| NM_001128845.1:c.2913G= | NP_001122317.1:p.Val971= | |
| NM_001128846.1:c.2913G= | NP_001122318.1:p.Val971= | |
| NM_001128847.1:c.2913G= | NP_001122319.1:p.Val971= | |
| NM_001128848.1:c.2913G= | NP_001122320.1:p.Val971= | |
| NM_001128849.1:c.2913G= | NP_001122321.1:p.Val971= | |
| NM_003072.3:c.2913G= | NP_003063.2:p.Val971= | |
| XM_005260028.2:c.2913G= | XP_005260085.1:p.Val971= | |
| XM_005260030.2:c.2913G= | XP_005260087.1:p.Val971= | |
| XM_005260031.2:c.2913G= | XP_005260088.1:p.Val971= | |
| XM_005260032.2:c.2913G= | XP_005260089.1:p.Val971= | |
| XM_005260033.2:c.2913G= | XP_005260090.1:p.Val971= | |
| XM_005260034.2:c.2913G= | XP_005260091.1:p.Val971= | |
| XM_005260035.2:c.2913G= | XP_005260092.1:p.Val971= | |
| XM_006722845.2:c.2913G= | XP_006722908.1:p.Val971= | |
| XM_006722846.2:c.2913G= | XP_006722909.1:p.Val971= | |
| XM_006722847.2:c.2913G= | XP_006722910.1:p.Val971= | |
| XM_011528198.1:c.2913G= | XP_011526500.1:p.Val971= | |
| XM_024451658.1:c.2913G= | XP_024307426.1:p.Val971= | |
| XM_024451659.1:c.2913G= | XP_024307427.1:p.Val971= | |
| XM_024451660.1:c.2913G= | XP_024307428.1:p.Val971= | |
| XM_024451661.1:c.2913G= | XP_024307429.1:p.Val971= | |
| XM_024451662.1:c.2913G= | XP_024307430.1:p.Val971= | |
| XM_024451663.1:c.2913G= | XP_024307431.1:p.Val971= | |
| XM_024451664.1:c.2913G= | XP_024307432.1:p.Val971= | |
| XM_024451665.1:c.2913G= | XP_024307433.1:p.Val971= | |
| XM_024451666.1:c.2913G= | XP_024307434.1:p.Val971= | |
| XM_024451667.1:c.2913G= | XP_024307435.1:p.Val971= | |
| NM_001128844.3:c.2913G= | NP_001122316.1:p.Val971= | |
| NM_001128845.2:c.2913G= | NP_001122317.1:p.Val971= | |
| NM_001128846.2:c.2913G= | NP_001122318.1:p.Val971= | |
| NM_001128847.4:c.2913G= | NP_001122319.1:p.Val971= | |
| NM_001128848.2:c.2913G= | NP_001122320.1:p.Val971= | |
| NM_001128849.3:c.2913G= | NP_001122321.1:p.Val971= | |
| NM_001374457.1:c.2913G= | NP_001361386.1:p.Val971= | |
| NM_003072.5:c.2913G= MANE Select | NP_003063.2:p.Val971= | |
| NR_164683.1:n.3203G= | ||
| NM_001387283.1:c.2913G= MANE Plus Clinical | NP_001374212.1:p.Val971= |