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_000020.11:g.44626447A= , CM000682.2:g.44626447A= | GRCh38 |
| NC_000020.10:g.43255088A= , CM000682.1:g.43255088A= | GRCh37 |
| NC_000020.9:g.42688502A= | NCBI36 |
| NG_007385.1:g.30289T= , LRG_16:g.30289T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000492931.6:n.453+9T= | ||
| ENST00000536076.2:c.209+9T= | ENSP00000512234.1:n.209+9T= | |
| ENST00000536532.6:c.362+9T= | ENSP00000440946.1:n.362+9T= | |
| ENST00000537820.2:c.362+9T= | ENSP00000441818.1:n.362+9T= | |
| ENST00000539235.6:c.218+2600T= | ENSP00000446464.1:n.218+2600T= | |
| ENST00000695889.1:c.218+2600T= | ENSP00000512240.1:n.218+2600T= | |
| ENST00000695890.1:n.2165+9T= | ||
| ENST00000695891.1:c.218+2600T= | ENSP00000512241.1:n.218+2600T= | |
| ENST00000695927.1:c.440+9T= | ENSP00000512270.1:n.440+9T= | |
| ENST00000695949.1:c.359+9T= | ENSP00000512281.1:n.359+9T= | |
| ENST00000695957.1:c.362+9T= | ENSP00000512286.1:n.362+9T= | |
| ENST00000695991.1:c.216+2602T= | ENSP00000512314.1:n.216+2602T= | |
| ENST00000695992.1:c.362+9T= | ENSP00000512315.1:n.362+9T= | |
| ENST00000695993.1:c.362+9T= | ENSP00000512316.1:n.362+9T= | |
| ENST00000695994.1:c.362+9T= | ENSP00000512317.1:n.362+9T= | |
| ENST00000695995.1:c.216+2602T= | ENSP00000512318.1:n.216+2602T= | |
| ENST00000695996.1:n.433+9T= | ||
| ENST00000695997.1:n.433+9T= | ||
| ENST00000696003.1:n.454+9T= | ||
| ENST00000696004.1:n.454+9T= | ||
| ENST00000696006.1:c.362+9T= | ENSP00000512325.1:n.362+9T= | |
| ENST00000696007.1:c.329+9T= | ENSP00000512326.1:n.329+9T= | |
| ENST00000696009.1:n.473+9T= | ||
| ENST00000696017.1:c.359+9T= | ENSP00000512333.1:n.359+9T= | |
| ENST00000696034.1:c.362+9T= | ENSP00000512343.1:n.362+9T= | |
| ENST00000696035.1:n.472+9T= | ||
| ENST00000696036.1:n.1052+9T= | ||
| ENST00000696037.1:n.2039+9T= | ||
| ENST00000696038.1:c.*108+9T= | ENSP00000512344.1:n.*108+9T= | |
| ENST00000696039.1:n.650+9T= | ||
| ENST00000696058.1:c.362+9T= | ENSP00000512361.1:n.362+9T= | |
| ENST00000696059.1:c.*307+9T= | ENSP00000512362.1:n.*307+9T= | |
| ENST00000696060.1:c.362+9T= | ENSP00000512363.1:n.362+9T= | |
| ENST00000696061.1:c.359+9T= | ENSP00000512364.1:n.359+9T= | |
| ENST00000696062.1:c.425+9T= | ENSP00000512365.1:n.425+9T= | |
| ENST00000696063.1:c.437+9T= | ENSP00000512366.1:n.437+9T= | |
| ENST00000696064.1:c.209+9T= | ENSP00000512367.1:n.209+9T= | |
| ENST00000696065.1:c.65+2600T= | ENSP00000512368.1:n.65+2600T= | |
| ENST00000696075.1:c.*332+9T= | ENSP00000512374.1:n.*332+9T= | |
| ENST00000696076.1:c.362+9T= | ENSP00000512375.1:n.362+9T= | |
| ENST00000696077.1:c.359+9T= | ENSP00000512376.1:n.359+9T= | |
| ENST00000696078.1:c.362+9T= | ENSP00000512377.1:n.362+9T= | |
| ENST00000696079.1:c.362+9T= | ENSP00000512378.1:n.362+9T= | |
| ENST00000696080.1:c.362+9T= | ENSP00000512379.1:n.362+9T= | |
| ENST00000696082.1:c.440+9T= | ENSP00000512380.1:n.440+9T= | |
| ENST00000696084.1:n.463+9T= | ||
| ENST00000696104.1:c.362+9T= | ENSP00000512399.1:n.362+9T= | |
| ENST00000696105.1:c.362+9T= | ENSP00000512400.1:n.362+9T= | |
| ENST00000372874.9:c.362+9T= MANE Select | ENSP00000361965.4:n.362+9T= | |
| ENST00000372874.8:c.362+9T= | ENSP00000361965.4:n.362+9T= | |
| ENST00000464097.5:n.36+9T= | ||
| ENST00000492931.5:n.446+9T= | ||
| ENST00000536532.5:c.362+9T= | ENSP00000440946.1:n.362+9T= | |
| ENST00000537820.1:c.362+9T= | ENSP00000441818.1:n.362+9T= | |
| ENST00000539235.5:c.218+2600T= | ENSP00000446464.1:n.218+2600T= | |
| ENST00000545776.5:n.425T= | ||
| NM_000022.2:c.362+9T= , LRG_16t1:c.362+9T= | NP_000013.2:n.362+9T= | |
| XM_005260236.2:c.362+9T= | XP_005260293.1:n.362+9T= | |
| XM_011528478.1:c.73+9T= | XP_011526780.1:n.73+9T= | |
| XM_011528479.1:c.73+9T= | XP_011526781.1:n.73+9T= | |
| XR_244129.1:n.416+9T= | ||
| NM_000022.3:c.362+9T= | NP_000013.2:n.362+9T= | |
| NM_001322050.1:c.73+9T= | NP_001308979.1:n.73+9T= | |
| NM_001322051.1:c.362+9T= | NP_001308980.1:n.362+9T= | |
| NR_136160.1:n.513+9T= | ||
| NM_000022.4:c.362+9T= MANE Select | NP_000013.2:n.362+9T= | |
| NM_001322050.2:c.73+9T= | NP_001308979.1:n.73+9T= | |
| NM_001322051.2:c.362+9T= | NP_001308980.1:n.362+9T= | |
| NR_136160.2:n.454+9T= |