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_000006.12:g.85507275T>C , CM000668.2:g.85507275T>C | GRCh38 |
| NC_000006.11:g.86216993T>C , CM000668.1:g.86216993T>C | GRCh37 |
| NC_000006.10:g.86273712T>C | NCBI36 |
| NG_047171.1:g.91882A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000418862.2:c.888A>G | ENSP00000391981.2:p.Leu296= | |
| ENST00000508658.6:c.2760A>G | ENSP00000422814.2:p.Leu920= | |
| ENST00000509338.6:c.1881A>G | ENSP00000424302.2:p.Leu627= | |
| ENST00000514801.2:n.1977A>G | ||
| ENST00000515216.6:c.2746-19A>G | ENSP00000425630.2:n.2746-19A>G | |
| ENST00000681965.1:c.3898A>G | ENSP00000507317.1:n.3898A>G | |
| ENST00000681981.1:c.2676A>G | ENSP00000507672.1:p.Leu892= | |
| ENST00000682022.1:c.*2652A>G | ENSP00000508118.1:n.*2652A>G | |
| ENST00000682023.1:c.*2383A>G | ENSP00000507998.1:n.*2383A>G | |
| ENST00000682034.1:c.*1927A>G | ENSP00000506724.1:n.*1927A>G | |
| ENST00000682057.1:c.*2189A>G | ENSP00000507883.1:n.*2189A>G | |
| ENST00000682083.1:c.*2670A>G | ENSP00000506859.1:n.*2670A>G | |
| ENST00000682106.1:n.5274A>G | ||
| ENST00000682133.1:c.*323A>G | ENSP00000507001.1:n.*323A>G | |
| ENST00000682171.1:c.2601A>G | ENSP00000508327.1:p.Leu867= | |
| ENST00000682174.1:c.*2383A>G | ENSP00000507248.1:n.*2383A>G | |
| ENST00000682374.1:c.*1306A>G | ENSP00000507425.1:n.*1306A>G | |
| ENST00000682412.1:c.2600A>G | ENSP00000507297.1:n.2600A>G | |
| ENST00000682454.1:c.*2123A>G | ENSP00000507851.1:n.*2123A>G | |
| ENST00000682455.1:c.*3738A>G | ENSP00000507586.1:n.*3738A>G | |
| ENST00000682464.1:c.*323A>G | ENSP00000507625.1:n.*323A>G | |
| ENST00000682491.1:c.2472A>G | ENSP00000506970.1:p.Leu824= | |
| ENST00000682497.1:c.2757A>G | ENSP00000507869.1:p.Leu919= | |
| ENST00000682504.1:c.*2666A>G | ENSP00000507623.1:n.*2666A>G | |
| ENST00000682514.1:n.8547A>G | ||
| ENST00000682594.1:n.3376A>G | ||
| ENST00000682633.1:c.*323A>G | ENSP00000507843.1:n.*323A>G | |
| ENST00000682660.1:c.2499A>G | ENSP00000507539.1:p.Leu833= | |
| ENST00000682682.1:c.2595A>G | ENSP00000507777.1:p.Leu865= | |
| ENST00000682688.1:c.*1765A>G | ENSP00000507097.1:n.*1765A>G | |
| ENST00000682694.1:c.*2123A>G | ENSP00000507387.1:n.*2123A>G | |
| ENST00000682709.1:n.8679A>G | ||
| ENST00000682738.1:c.2568A>G | ENSP00000507742.1:p.Leu856= | |
| ENST00000682776.1:c.*1511A>G | ENSP00000507490.1:n.*1511A>G | |
| ENST00000682854.1:c.*2748A>G | ENSP00000507257.1:n.*2748A>G | |
| ENST00000682878.1:c.*2448A>G | ENSP00000507360.1:n.*2448A>G | |
| ENST00000682926.1:n.2167A>G | ||
| ENST00000682939.1:c.2472A>G | ENSP00000506902.1:p.Leu824= | |
| ENST00000682991.1:c.2541A>G | ENSP00000508193.1:p.Leu847= | |
| ENST00000682995.1:c.*1484A>G | ENSP00000506807.1:n.*1484A>G | |
| ENST00000683073.1:c.*878A>G | ENSP00000507270.1:n.*878A>G | |
| ENST00000683074.1:c.*2670A>G | ENSP00000507008.1:n.*2670A>G | |
| ENST00000683085.1:c.*835A>G | ENSP00000507993.1:n.*835A>G | |
| ENST00000683097.1:c.*1130A>G | ENSP00000507556.1:n.*1130A>G | |
| ENST00000683126.1:c.*2280A>G | ENSP00000507507.1:n.*2280A>G | |
| ENST00000683195.1:c.*2123A>G | ENSP00000508190.1:n.*2123A>G | |
| ENST00000683196.1:c.*2123A>G | ENSP00000508297.1:n.*2123A>G | |
| ENST00000683364.1:c.*2630A>G | ENSP00000507791.1:n.*2630A>G | |
| ENST00000683436.1:c.*1791A>G | ENSP00000506874.1:n.*1791A>G | |
| ENST00000683458.1:c.*1511A>G | ENSP00000508204.1:n.*1511A>G | |
| ENST00000683473.1:n.3871A>G | ||
| ENST00000683479.1:c.2760A>G | ENSP00000507368.1:p.Leu920= | |
| ENST00000683481.1:c.*1642A>G | ENSP00000507015.1:n.*1642A>G | |
| ENST00000683541.1:c.2757A>G | ENSP00000507116.1:p.Leu919= | |
| ENST00000683542.1:c.*2284A>G | ENSP00000506893.1:n.*2284A>G | |
| ENST00000683577.1:c.*323A>G | ENSP00000507516.1:n.*323A>G | |
| ENST00000683583.1:c.*5174A>G | ENSP00000507244.1:n.*5174A>G | |
| ENST00000683643.1:c.2628A>G | ENSP00000507444.1:p.Leu876= | |
| ENST00000683698.1:c.*2276A>G | ENSP00000507000.1:n.*2276A>G | |
| ENST00000683726.1:c.*2280A>G | ENSP00000507744.1:n.*2280A>G | |
| ENST00000683754.1:c.2679A>G | ENSP00000507707.1:p.Leu893= | |
| ENST00000683763.1:n.1458A>G | ||
| ENST00000683785.1:c.2625A>G | ENSP00000507188.1:p.Leu875= | |
| ENST00000683803.1:c.*1511A>G | ENSP00000508216.1:n.*1511A>G | |
| ENST00000683857.1:c.*2189A>G | ENSP00000508015.1:n.*2189A>G | |
| ENST00000683873.1:c.*2335A>G | ENSP00000506829.1:n.*2335A>G | |
| ENST00000683878.1:c.*2041A>G | ENSP00000507449.1:n.*2041A>G | |
| ENST00000683880.1:c.*2284A>G | ENSP00000508357.1:n.*2284A>G | |
| ENST00000683898.1:c.2595A>G | ENSP00000506897.1:p.Leu865= | |
| ENST00000683909.1:n.4790A>G | ||
| ENST00000684017.1:n.8272A>G | ||
| ENST00000684108.1:n.8679A>G | ||
| ENST00000684118.1:c.2743-19A>G | ENSP00000507950.1:n.2743-19A>G | |
| ENST00000684150.1:c.2601A>G | ENSP00000507401.1:p.Leu867= | |
| ENST00000684220.1:c.*2630A>G | ENSP00000507382.1:n.*2630A>G | |
| ENST00000684239.1:c.*2385A>G | ENSP00000507479.1:n.*2385A>G | |
| ENST00000684273.1:c.*2253A>G | ENSP00000508063.1:n.*2253A>G | |
| ENST00000684281.1:c.2409A>G | ENSP00000507932.1:p.Leu803= | |
| ENST00000684299.1:c.*323A>G | ENSP00000507637.1:n.*323A>G | |
| ENST00000684319.1:c.*323A>G | ENSP00000508346.1:n.*323A>G | |
| ENST00000684422.1:c.*2433A>G | ENSP00000507146.1:n.*2433A>G | |
| ENST00000684451.1:c.*2065A>G | ENSP00000507384.1:n.*2065A>G | |
| ENST00000684570.1:c.2823A>G | ENSP00000508127.1:p.Leu941= | |
| ENST00000684581.1:c.*581A>G | ENSP00000507294.1:n.*581A>G | |
| ENST00000684647.1:c.2469A>G | ENSP00000506873.1:p.Leu823= | |
| ENST00000684680.1:c.2385A>G | ENSP00000507491.1:p.Leu795= | |
| ENST00000684717.1:c.2877A>G | ENSP00000507024.1:p.Leu959= | |
| ENST00000314673.8:c.2760A>G MANE Select | ENSP00000313121.3:p.Leu920= | |
| ENST00000314673.7:c.2760A>G | ENSP00000313121.3:p.Leu920= | |
| ENST00000346348.7:c.2601A>G | ENSP00000257769.3:p.Leu867= | |
| ENST00000369627.6:c.2733A>G | ENSP00000358641.2:p.Leu911= | |
| ENST00000474645.6:n.505A>G | ||
| ENST00000503491.5:n.3249A>G | ||
| ENST00000505648.5:c.2604A>G | ENSP00000427380.1:p.Leu868= | |
| ENST00000508658.5:c.476A>G | ||
| ENST00000508980.5:n.3366A>G | ||
| ENST00000513865.5:c.1917A>G | ENSP00000420938.1:p.Leu639= | |
| NM_001297614.2:c.2733A>G | NP_001284543.1:p.Leu911= | |
| NM_001304479.1:c.2604A>G | NP_001291408.1:p.Leu868= | |
| NM_020468.5:c.2601A>G | NP_065201.1:p.Leu867= | |
| NM_153816.5:c.2760A>G | NP_722523.1:p.Leu920= | |
| XM_005248738.3:c.2757A>G | XP_005248795.1:p.Leu919= | |
| XM_005248740.3:c.2628A>G | XP_005248797.1:p.Leu876= | |
| XM_011535978.1:c.2541A>G | XP_011534280.1:p.Leu847= | |
| XM_011535979.1:c.2472A>G | XP_011534281.1:p.Leu824= | |
| XM_011535980.1:c.1605A>G | XP_011534282.1:p.Leu535= | |
| XR_942523.1:n.2868A>G | ||
| NM_001350532.1:c.2823A>G | NP_001337461.1:p.Leu941= | |
| NM_001350533.1:c.2757A>G | NP_001337462.1:p.Leu919= | |
| NM_001350534.1:c.2730A>G | NP_001337463.1:p.Leu910= | |
| NM_001350535.1:c.2743-19A>G | NP_001337464.1:n.2743-19A>G | |
| NM_001350536.1:c.2628A>G | NP_001337465.1:p.Leu876= | |
| NM_001350537.1:c.2625A>G | NP_001337466.1:p.Leu875= | |
| NM_001350538.1:c.2616A>G | NP_001337467.1:p.Leu872= | |
| NM_001350539.1:c.2601A>G | NP_001337468.1:p.Leu867= | |
| NM_001350540.1:c.2595A>G | NP_001337469.1:p.Leu865= | |
| NM_001350541.1:c.2568A>G | NP_001337470.1:p.Leu856= | |
| NM_001350542.1:c.2472A>G | NP_001337471.1:p.Leu824= | |
| NM_001350543.1:c.2469A>G | NP_001337472.1:p.Leu823= | |
| NM_001350544.1:c.2460A>G | NP_001337473.1:p.Leu820= | |
| NM_001350545.1:c.2316A>G | NP_001337474.1:p.Leu772= | |
| NM_001350546.1:c.2316A>G | NP_001337475.1:p.Leu772= | |
| NM_001350547.1:c.1710A>G | NP_001337476.1:p.Leu570= | |
| NM_001350548.1:c.1605A>G | NP_001337477.1:p.Leu535= | |
| NM_001350549.1:c.1605A>G | NP_001337478.1:p.Leu535= | |
| NM_001350550.1:c.1605A>G | NP_001337479.1:p.Leu535= | |
| NM_001350551.1:c.1605A>G | NP_001337480.1:p.Leu535= | |
| NM_001350552.1:c.1605A>G | NP_001337481.1:p.Leu535= | |
| NM_001350553.1:c.1578A>G | NP_001337482.1:p.Leu526= | |
| NR_146774.1:n.3194A>G | ||
| NR_146775.1:n.3197A>G | ||
| NR_146776.1:n.3320A>G | ||
| NR_146777.1:n.3448A>G | ||
| NR_146778.1:n.3452A>G | ||
| NR_146779.1:n.3449A>G | ||
| XM_017011090.1:c.2601A>G | XP_016866579.1:p.Leu867= | |
| XM_024446498.1:c.2469A>G | XP_024302266.1:p.Leu823= | |
| XM_024446499.1:c.1605A>G | XP_024302267.1:p.Leu535= | |
| NM_153816.6:c.2760A>G MANE Select | NP_722523.1:p.Leu920= | |
| NM_001297614.3:c.2733A>G | NP_001284543.1:p.Leu911= | |
| NM_001304479.2:c.2604A>G | NP_001291408.1:p.Leu868= | |
| NM_001350532.2:c.2823A>G | NP_001337461.1:p.Leu941= | |
| NM_001350533.2:c.2757A>G | NP_001337462.1:p.Leu919= | |
| NM_001350534.2:c.2730A>G | NP_001337463.1:p.Leu910= | |
| NM_001350535.2:c.2743-19A>G | NP_001337464.1:n.2743-19A>G | |
| NM_001350536.2:c.2628A>G | NP_001337465.1:p.Leu876= | |
| NM_001350537.2:c.2625A>G | NP_001337466.1:p.Leu875= | |
| NM_001350538.2:c.2616A>G | NP_001337467.1:p.Leu872= | |
| NM_001350539.2:c.2601A>G | NP_001337468.1:p.Leu867= | |
| NM_001350540.2:c.2595A>G | NP_001337469.1:p.Leu865= | |
| NM_001350541.2:c.2568A>G | NP_001337470.1:p.Leu856= | |
| NM_001350542.2:c.2472A>G | NP_001337471.1:p.Leu824= | |
| NM_001350543.2:c.2469A>G | NP_001337472.1:p.Leu823= | |
| NM_001350544.2:c.2460A>G | NP_001337473.1:p.Leu820= | |
| NM_001350545.2:c.2316A>G | NP_001337474.1:p.Leu772= | |
| NM_001350546.2:c.2316A>G | NP_001337475.1:p.Leu772= | |
| NM_001350547.2:c.1710A>G | NP_001337476.1:p.Leu570= | |
| NM_001350548.2:c.1605A>G | NP_001337477.1:p.Leu535= | |
| NM_001350549.2:c.1605A>G | NP_001337478.1:p.Leu535= | |
| NM_001350550.2:c.1605A>G | NP_001337479.1:p.Leu535= | |
| NM_001350551.2:c.1605A>G | NP_001337480.1:p.Leu535= | |
| NM_001350552.2:c.1605A>G | NP_001337481.1:p.Leu535= | |
| NM_001350553.2:c.1578A>G | NP_001337482.1:p.Leu526= | |
| NM_020468.6:c.2601A>G | NP_065201.1:p.Leu867= | |
| NR_146774.2:n.2896A>G | ||
| NR_146775.2:n.2899A>G | ||
| NR_146776.2:n.3022A>G | ||
| NR_146777.2:n.3150A>G | ||
| NR_146778.2:n.3154A>G | ||
| NR_146779.2:n.3151A>G |