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.11023559T= , CM000681.2:g.11023559T= | GRCh38 |
| NC_000019.9:g.11134235T= , CM000681.1:g.11134235T= | GRCh37 |
| NC_000019.8:g.10995235T= | NCBI36 |
| NG_011556.2:g.67638T= | |
| NG_011556.3:g.67628T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000711079.1:c.2901T= | ENSP00000518564.1:p.Arg967= | |
| ENST00000704344.1:c.2901T= | ENSP00000515855.1:p.Arg967= | |
| ENST00000704345.1:c.2892T= | ENSP00000515856.1:p.Arg964= | |
| ENST00000646693.2:c.2901T= MANE Plus Clinical | ENSP00000495368.1:p.Arg967= | |
| ENST00000344626.10:c.2901T= MANE Select | ENSP00000343896.4:p.Arg967= | |
| ENST00000429416.8:c.2901T= | ENSP00000395654.1:p.Arg967= | |
| ENST00000444061.8:c.2901T= | ENSP00000392837.2:p.Arg967= | |
| ENST00000590574.6:c.2901T= | ENSP00000466963.1:p.Arg967= | |
| ENST00000591545.6:c.2774T= | ||
| ENST00000592604.6:n.1232T= | ||
| ENST00000642350.1:c.1386T= | ENSP00000495355.1:p.Arg462= | |
| ENST00000642508.1:c.262T= | ||
| ENST00000642628.1:c.2901T= | ENSP00000496498.1:p.Arg967= | |
| ENST00000642726.1:c.2901T= | ENSP00000494353.1:p.Arg967= | |
| ENST00000643208.1:c.1458T= | ENSP00000496074.1:p.Arg486= | |
| ENST00000643296.1:c.2901T= | ENSP00000496635.1:p.Arg967= | |
| ENST00000643534.1:c.1186T= | ||
| ENST00000643549.1:c.2901T= | ENSP00000493975.1:p.Arg967= | |
| ENST00000643857.1:c.1256T= | ||
| ENST00000643995.1:c.2315T= | ||
| ENST00000644065.1:c.1628T= | ||
| ENST00000644267.1:n.1256T= | ||
| ENST00000644290.1:c.1158T= | ||
| ENST00000644327.1:c.1672T= | ||
| ENST00000644737.1:c.2901T= | ENSP00000495548.1:p.Arg967= | |
| ENST00000644963.1:c.1546T= | ||
| ENST00000645061.1:c.1389T= | ENSP00000493690.1:p.Arg463= | |
| ENST00000645460.1:c.2901T= | ENSP00000494463.1:p.Arg967= | |
| ENST00000645648.1:c.765T= | ENSP00000493521.1:p.Arg255= | |
| ENST00000646183.1:c.1247T= | ||
| ENST00000646236.1:c.384T= | ENSP00000493925.1:p.Arg128= | |
| ENST00000646484.1:c.2901T= | ENSP00000495536.1:p.Arg967= | |
| ENST00000646510.1:c.2901T= | ENSP00000494772.1:p.Arg967= | |
| ENST00000646513.1:c.735T= | ENSP00000495457.1:p.Arg245= | |
| ENST00000646593.1:c.749T= | ENSP00000494341.1:n.749T= | |
| ENST00000646693.1:c.2901T= | ENSP00000495368.1:p.Arg967= | |
| ENST00000646746.1:c.1201T= | ||
| ENST00000647230.1:c.2901T= | ENSP00000494676.1:p.Arg967= | |
| ENST00000647268.1:c.1254T= | ENSP00000496176.1:p.Arg418= | |
| ENST00000344626.8:c.2901T= | ENSP00000343896.4:p.Arg967= | |
| ENST00000413806.7:c.3093T= | ENSP00000414727.3:p.Arg1031= | |
| ENST00000429416.7:c.2901T= | ENSP00000395654.1:p.Arg967= | |
| ENST00000444061.7:c.2901T= | ENSP00000392837.2:p.Arg967= | |
| ENST00000450717.7:c.2901T= | ENSP00000397783.3:p.Arg967= | |
| ENST00000541122.6:c.2901T= | ENSP00000445036.2:p.Arg967= | |
| ENST00000585799.5:n.1429T= | ||
| ENST00000586122.5:n.483T= | ||
| ENST00000587988.5:n.550T= | ||
| ENST00000589677.5:c.2901T= | ENSP00000464778.1:p.Arg967= | |
| ENST00000590574.5:c.2901T= | ENSP00000466963.1:p.Arg967= | |
| ENST00000591545.5:n.2775T= | ||
| ENST00000591595.5:n.973T= | ||
| ENST00000592604.5:n.814T= | ||
| NM_001128844.1:c.2901T= | NP_001122316.1:p.Arg967= | |
| NM_001128845.1:c.2901T= | NP_001122317.1:p.Arg967= | |
| NM_001128846.1:c.2901T= | NP_001122318.1:p.Arg967= | |
| NM_001128847.1:c.2901T= | NP_001122319.1:p.Arg967= | |
| NM_001128848.1:c.2901T= | NP_001122320.1:p.Arg967= | |
| NM_001128849.1:c.2901T= | NP_001122321.1:p.Arg967= | |
| NM_003072.3:c.2901T= | NP_003063.2:p.Arg967= | |
| XM_005260028.2:c.2901T= | XP_005260085.1:p.Arg967= | |
| XM_005260030.2:c.2901T= | XP_005260087.1:p.Arg967= | |
| XM_005260031.2:c.2901T= | XP_005260088.1:p.Arg967= | |
| XM_005260032.2:c.2901T= | XP_005260089.1:p.Arg967= | |
| XM_005260033.2:c.2901T= | XP_005260090.1:p.Arg967= | |
| XM_005260034.2:c.2901T= | XP_005260091.1:p.Arg967= | |
| XM_005260035.2:c.2901T= | XP_005260092.1:p.Arg967= | |
| XM_006722845.2:c.2901T= | XP_006722908.1:p.Arg967= | |
| XM_006722846.2:c.2901T= | XP_006722909.1:p.Arg967= | |
| XM_006722847.2:c.2901T= | XP_006722910.1:p.Arg967= | |
| XM_011528198.1:c.2901T= | XP_011526500.1:p.Arg967= | |
| XM_024451658.1:c.2901T= | XP_024307426.1:p.Arg967= | |
| XM_024451659.1:c.2901T= | XP_024307427.1:p.Arg967= | |
| XM_024451660.1:c.2901T= | XP_024307428.1:p.Arg967= | |
| XM_024451661.1:c.2901T= | XP_024307429.1:p.Arg967= | |
| XM_024451662.1:c.2901T= | XP_024307430.1:p.Arg967= | |
| XM_024451663.1:c.2901T= | XP_024307431.1:p.Arg967= | |
| XM_024451664.1:c.2901T= | XP_024307432.1:p.Arg967= | |
| XM_024451665.1:c.2901T= | XP_024307433.1:p.Arg967= | |
| XM_024451666.1:c.2901T= | XP_024307434.1:p.Arg967= | |
| XM_024451667.1:c.2901T= | XP_024307435.1:p.Arg967= | |
| NM_001128844.3:c.2901T= | NP_001122316.1:p.Arg967= | |
| NM_001128845.2:c.2901T= | NP_001122317.1:p.Arg967= | |
| NM_001128846.2:c.2901T= | NP_001122318.1:p.Arg967= | |
| NM_001128847.4:c.2901T= | NP_001122319.1:p.Arg967= | |
| NM_001128848.2:c.2901T= | NP_001122320.1:p.Arg967= | |
| NM_001128849.3:c.2901T= | NP_001122321.1:p.Arg967= | |
| NM_001374457.1:c.2901T= | NP_001361386.1:p.Arg967= | |
| NM_003072.5:c.2901T= MANE Select | NP_003063.2:p.Arg967= | |
| NR_164683.1:n.3191T= | ||
| NM_001387283.1:c.2901T= MANE Plus Clinical | NP_001374212.1:p.Arg967= |