WARNING - Protein Allele ID and Protein Sequence HGVS API Requests Temporarily Disabled:
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
We are investigating the periodic unresponsiveness in the Registry.
Although replication attempts were unsuccessful, there is a high correlation with protein alleles. And with haplotype HGVS queries.
This temporarily affects the API and the UI.
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.17393561C= , CM000673.2:g.17393561C= | GRCh38 |
| NC_000011.9:g.17415108C= , CM000673.1:g.17415108C= | GRCh37 |
| NC_000011.8:g.17371684C= | NCBI36 |
| NG_008867.1:g.88342G= | |
| NG_012446.1:g.99G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000524561.2:n.4209+136G= | ||
| ENST00000526037.6:n.543+136G= | ||
| ENST00000528374.2:c.1199+136G= | ||
| ENST00000529967.6:n.2947+136G= | ||
| ENST00000532220.2:n.3841+136G= | ||
| ENST00000642611.2:n.5941+136G= | ||
| ENST00000644057.2:n.1184+136G= | ||
| ENST00000645004.2:n.2107+136G= | ||
| ENST00000682051.1:n.4770+136G= | ||
| ENST00000682110.1:n.4823+136G= | ||
| ENST00000682140.1:c.*394+136G= | ENSP00000507829.1:n.*394+136G= | |
| ENST00000682185.1:n.5913+136G= | ||
| ENST00000682204.1:c.*2746+136G= | ENSP00000507094.1:n.*2746+136G= | |
| ENST00000682215.1:n.5190+136G= | ||
| ENST00000682288.1:c.*3039+136G= | ENSP00000507506.1:n.*3039+136G= | |
| ENST00000682442.1:n.5043+136G= | ||
| ENST00000682528.1:n.4900+136G= | ||
| ENST00000682673.1:n.4767+136G= | ||
| ENST00000682805.1:n.5228+136G= | ||
| ENST00000682965.1:c.*1030+136G= | ENSP00000508229.1:n.*1030+136G= | |
| ENST00000683093.1:n.5803+136G= | ||
| ENST00000683136.1:c.4491+136G= | ENSP00000507768.1:n.4491+136G= | |
| ENST00000683153.1:n.4865+136G= | ||
| ENST00000683365.1:n.4925+136G= | ||
| ENST00000683377.1:n.4719+136G= | ||
| ENST00000683456.1:c.*1745+136G= | ENSP00000508318.1:n.*1745+136G= | |
| ENST00000683522.1:n.4905+136G= | ||
| ENST00000683562.1:c.*2673+136G= | ENSP00000508265.1:n.*2673+136G= | |
| ENST00000683693.1:n.6284+136G= | ||
| ENST00000683725.1:c.*73+136G= | ENSP00000507496.1:n.*73+136G= | |
| ENST00000684010.1:n.4818+136G= | ||
| ENST00000684014.1:n.795+136G= | ||
| ENST00000684157.1:n.5808+136G= | ||
| ENST00000684253.1:n.4726+136G= | ||
| ENST00000684288.1:c.*2780+136G= | ENSP00000507143.1:n.*2780+136G= | |
| ENST00000684313.1:n.4255+136G= | ||
| ENST00000684332.1:n.4896+136G= | ||
| ENST00000684371.1:n.4929+136G= | ||
| ENST00000684404.1:n.5851+136G= | ||
| ENST00000684442.1:n.5047+136G= | ||
| ENST00000684555.1:c.*2820+136G= | ENSP00000507705.1:n.*2820+136G= | |
| ENST00000684571.1:c.4449+136G= | ENSP00000506935.1:n.4449+136G= | |
| ENST00000684593.1:c.*4313+136G= | ENSP00000507005.1:n.*4313+136G= | |
| ENST00000684711.1:c.*3004+136G= | ENSP00000506841.1:n.*3004+136G= | |
| ENST00000302539.9:c.4611+136G= | ENSP00000303960.4:n.4611+136G= | |
| ENST00000389817.8:c.4608+136G= MANE Select | ENSP00000374467.4:n.4608+136G= | |
| ENST00000642271.1:c.4605+136G= | ENSP00000493749.1:n.4605+136G= | |
| ENST00000642579.1:c.2662+136G= | ||
| ENST00000642611.1:n.5826+136G= | ||
| ENST00000642902.1:c.4390+136G= | ||
| ENST00000643260.1:c.4608+136G= | ENSP00000494450.1:n.4608+136G= | |
| ENST00000643562.1:c.*2730+136G= | ENSP00000496124.1:n.*2730+136G= | |
| ENST00000643925.1:c.3186-433G= | ||
| ENST00000644057.1:n.767+136G= | ||
| ENST00000644484.1:c.*3994+136G= | ENSP00000493558.1:n.*3994+136G= | |
| ENST00000644675.1:c.*2780+136G= | ENSP00000494567.1:n.*2780+136G= | |
| ENST00000644757.1:c.*3203-581G= | ENSP00000495085.1:n.*3203-581G= | |
| ENST00000644772.1:c.4674+136G= | ENSP00000494321.1:n.4674+136G= | |
| ENST00000645004.1:n.2301+136G= | ||
| ENST00000645076.1:c.3703+136G= | ||
| ENST00000645417.1:c.1796+136G= | ||
| ENST00000645744.1:c.*4293+136G= | ENSP00000494564.1:n.*4293+136G= | |
| ENST00000645760.1:c.5029+136G= | ||
| ENST00000645884.1:c.*1891+136G= | ENSP00000495516.1:n.*1891+136G= | |
| ENST00000646003.1:c.*2630+136G= | ENSP00000495259.1:n.*2630+136G= | |
| ENST00000646207.1:c.*3445+136G= | ENSP00000495025.1:n.*3445+136G= | |
| ENST00000646276.1:c.*4012+136G= | ENSP00000496070.1:n.*4012+136G= | |
| ENST00000646592.1:c.3914+136G= | ||
| ENST00000646902.1:c.4575+136G= | ENSP00000494101.1:n.4575+136G= | |
| ENST00000646993.1:c.*3046+136G= | ENSP00000493720.1:n.*3046+136G= | |
| ENST00000647015.1:c.4359+136G= | ENSP00000495389.1:n.4359+136G= | |
| ENST00000647086.1:c.*4194+136G= | ENSP00000493677.1:n.*4194+136G= | |
| ENST00000647158.1:c.*2895+136G= | ENSP00000495744.1:n.*2895+136G= | |
| ENST00000302539.8:c.4611+136G= | ENSP00000303960.4:n.4611+136G= | |
| ENST00000389817.7:c.4608+136G= | ENSP00000374467.3:n.4608+136G= | |
| ENST00000525022.1:n.503+136G= | ||
| ENST00000526037.5:n.368+136G= | ||
| ENST00000526168.5:c.396+136G= | ||
| ENST00000531642.5:c.639+136G= | ||
| NM_000352.4:c.4608+136G= | NP_000343.2:n.4608+136G= | |
| NM_001287174.1:c.4611+136G= | NP_001274103.1:n.4611+136G= | |
| XM_011520331.1:c.4608+136G= | XP_011518633.1:n.4608+136G= | |
| XM_011520333.1:c.3108+136G= | XP_011518635.1:n.3108+136G= | |
| XR_930890.1:n.4570+136G= | ||
| NM_001351295.1:c.4674+136G= | NP_001338224.1:n.4674+136G= | |
| NM_001351296.1:c.4608+136G= | NP_001338225.1:n.4608+136G= | |
| NM_001351297.1:c.4605+136G= | NP_001338226.1:n.4605+136G= | |
| NR_147094.1:n.4903+136G= | ||
| XM_017018197.2:c.4677+136G= | XP_016873686.1:n.4677+136G= | |
| XM_017018199.1:c.4674+136G= | XP_016873688.1:n.4674+136G= | |
| XM_017018202.1:c.3174+136G= | XP_016873691.1:n.3174+136G= | |
| XM_017018204.1:c.2565+136G= | XP_016873693.1:n.2565+136G= | |
| XM_024448668.1:c.2976+136G= | XP_024304436.1:n.2976+136G= | |
| XR_001747945.2:n.4645+136G= | ||
| XR_001747946.2:n.4576+136G= | ||
| XR_002957189.1:n.6359+136G= | ||
| NM_000352.6:c.4608+136G= MANE Select | NP_000343.2:n.4608+136G= | |
| NM_001287174.2:c.4611+136G= | NP_001274103.1:n.4611+136G= | |
| NM_001351295.2:c.4674+136G= | NP_001338224.1:n.4674+136G= | |
| NM_001351296.2:c.4608+136G= | NP_001338225.1:n.4608+136G= | |
| NM_001351297.2:c.4605+136G= | NP_001338226.1:n.4605+136G= | |
| NR_147094.2:n.4903+136G= | ||
| NM_001287174.3:c.4611+136G= | NP_001274103.1:n.4611+136G= |