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_000011.10:g.17406892C= , CM000673.2:g.17406892C= | GRCh38 |
| NC_000011.9:g.17428439C= , CM000673.1:g.17428439C= | GRCh37 |
| NC_000011.8:g.17385015C= | NCBI36 |
| NG_008867.1:g.75011G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000524561.2:n.2727G= | ||
| ENST00000529967.6:n.1497G= | ||
| ENST00000532220.2:n.890G= | ||
| ENST00000642611.2:n.3227G= | ||
| ENST00000645004.2:n.657G= | ||
| ENST00000682051.1:n.3174G= | ||
| ENST00000682110.1:n.3227G= | ||
| ENST00000682140.1:c.3155G= | ENSP00000507829.1:p.Ser1052= | |
| ENST00000682185.1:n.4463G= | ||
| ENST00000682204.1:c.*1296G= | ENSP00000507094.1:n.*1296G= | |
| ENST00000682215.1:n.3224G= | ||
| ENST00000682288.1:c.*1589G= | ENSP00000507506.1:n.*1589G= | |
| ENST00000682442.1:n.3348G= | ||
| ENST00000682528.1:n.3304G= | ||
| ENST00000682673.1:n.3171G= | ||
| ENST00000682805.1:n.3224G= | ||
| ENST00000682965.1:c.3155G= | ENSP00000508229.1:p.Ser1052= | |
| ENST00000683093.1:n.3326G= | ||
| ENST00000683136.1:c.3155G= | ENSP00000507768.1:p.Ser1052= | |
| ENST00000683153.1:n.3383G= | ||
| ENST00000683365.1:n.3329G= | ||
| ENST00000683377.1:n.3227G= | ||
| ENST00000683456.1:c.*295G= | ENSP00000508318.1:n.*295G= | |
| ENST00000683522.1:n.3227G= | ||
| ENST00000683562.1:c.*1327G= | ENSP00000508265.1:n.*1327G= | |
| ENST00000683693.1:n.3304G= | ||
| ENST00000683725.1:c.3158G= | ENSP00000507496.1:p.Ser1053= | |
| ENST00000684010.1:n.3222G= | ||
| ENST00000684157.1:n.3227G= | ||
| ENST00000684253.1:n.3130G= | ||
| ENST00000684288.1:c.*1330G= | ENSP00000507143.1:n.*1330G= | |
| ENST00000684313.1:n.2659G= | ||
| ENST00000684332.1:n.3300G= | ||
| ENST00000684371.1:n.3333G= | ||
| ENST00000684404.1:n.3270G= | ||
| ENST00000684442.1:n.3227G= | ||
| ENST00000684555.1:c.*1370G= | ENSP00000507705.1:n.*1370G= | |
| ENST00000684571.1:c.2999G= | ENSP00000506935.1:p.Ser1000= | |
| ENST00000684593.1:c.*2863G= | ENSP00000507005.1:n.*2863G= | |
| ENST00000684711.1:c.*1554G= | ENSP00000506841.1:n.*1554G= | |
| ENST00000302539.9:c.3161G= | ENSP00000303960.4:p.Ser1054= | |
| ENST00000389817.8:c.3158G= MANE Select | ENSP00000374467.4:p.Ser1053= | |
| ENST00000642271.1:c.3155G= | ENSP00000493749.1:p.Ser1052= | |
| ENST00000642579.1:c.1242G= | ||
| ENST00000642611.1:n.3112G= | ||
| ENST00000642902.1:c.2940G= | ||
| ENST00000643260.1:c.3158G= | ENSP00000494450.1:p.Ser1053= | |
| ENST00000643562.1:c.*1134G= | ENSP00000496124.1:n.*1134G= | |
| ENST00000643925.1:c.1282G= | ||
| ENST00000644447.1:c.1514G= | ENSP00000496282.1:p.Ser505= | |
| ENST00000644484.1:c.*1413G= | ENSP00000493558.1:n.*1413G= | |
| ENST00000644542.1:c.*2863G= | ENSP00000495532.1:n.*2863G= | |
| ENST00000644675.1:c.*1330G= | ENSP00000494567.1:n.*1330G= | |
| ENST00000644757.1:c.*1443G= | ENSP00000495085.1:n.*1443G= | |
| ENST00000644772.1:c.3224G= | ENSP00000494321.1:p.Ser1075= | |
| ENST00000645004.1:n.297G= | ||
| ENST00000645076.1:c.2357G= | ||
| ENST00000645417.1:c.324G= | ||
| ENST00000645744.1:c.*1422G= | ENSP00000494564.1:n.*1422G= | |
| ENST00000645760.1:c.3433G= | ||
| ENST00000645884.1:c.*295G= | ENSP00000495516.1:n.*295G= | |
| ENST00000646003.1:c.*1114G= | ENSP00000495259.1:n.*1114G= | |
| ENST00000646207.1:c.*1625G= | ENSP00000495025.1:n.*1625G= | |
| ENST00000646276.1:c.*1431G= | ENSP00000496070.1:n.*1431G= | |
| ENST00000646592.1:c.2464G= | ||
| ENST00000646902.1:c.3155G= | ENSP00000494101.1:p.Ser1052= | |
| ENST00000646993.1:c.*1554G= | ENSP00000493720.1:n.*1554G= | |
| ENST00000647013.1:c.3164G= | ENSP00000496741.1:n.3164G= | |
| ENST00000647015.1:c.2909G= | ENSP00000495389.1:p.Ser970= | |
| ENST00000647086.1:c.*2888G= | ENSP00000493677.1:n.*2888G= | |
| ENST00000647158.1:c.*1299G= | ENSP00000495744.1:n.*1299G= | |
| ENST00000302539.8:c.3161G= | ENSP00000303960.4:p.Ser1054= | |
| ENST00000389817.7:c.3158G= | ENSP00000374467.3:p.Ser1053= | |
| ENST00000524561.1:n.290G= | ||
| ENST00000526921.5:n.842G= | ||
| ENST00000527905.5:c.*34G= | ENSP00000431653.1:n.*34G= | |
| ENST00000529967.5:n.827G= | ||
| NM_000352.4:c.3158G= | NP_000343.2:p.Ser1053= | |
| NM_001287174.1:c.3161G= | NP_001274103.1:p.Ser1054= | |
| XM_011520331.1:c.3158G= | XP_011518633.1:p.Ser1053= | |
| XM_011520332.1:c.3161G= | XP_011518634.1:p.Ser1054= | |
| XM_011520333.1:c.1658G= | XP_011518635.1:p.Ser553= | |
| XR_930890.1:n.3224G= | ||
| XR_930891.1:n.3224G= | ||
| XR_930892.1:n.3124G= | ||
| XR_930893.1:n.3121G= | ||
| NM_001351295.1:c.3224G= | NP_001338224.1:p.Ser1075= | |
| NM_001351296.1:c.3158G= | NP_001338225.1:p.Ser1053= | |
| NM_001351297.1:c.3155G= | NP_001338226.1:p.Ser1052= | |
| NR_147094.1:n.3307G= | ||
| XM_017018197.2:c.3227G= | XP_016873686.1:p.Ser1076= | |
| XM_017018199.1:c.3224G= | XP_016873688.1:p.Ser1075= | |
| XM_017018201.2:c.3227G= | XP_016873690.1:p.Ser1076= | |
| XM_017018202.1:c.1724G= | XP_016873691.1:p.Ser575= | |
| XM_017018204.1:c.1115G= | XP_016873693.1:p.Ser372= | |
| XM_024448668.1:c.1526G= | XP_024304436.1:p.Ser509= | |
| XR_001747945.2:n.3299G= | ||
| XR_001747946.2:n.3230G= | ||
| XR_002957189.1:n.3379G= | ||
| NM_000352.6:c.3158G= MANE Select | NP_000343.2:p.Ser1053= | |
| NM_001287174.2:c.3161G= | NP_001274103.1:p.Ser1054= | |
| NM_001351295.2:c.3224G= | NP_001338224.1:p.Ser1075= | |
| NM_001351296.2:c.3158G= | NP_001338225.1:p.Ser1053= | |
| NM_001351297.2:c.3155G= | NP_001338226.1:p.Ser1052= | |
| NR_147094.2:n.3307G= | ||
| NM_001287174.3:c.3161G= | NP_001274103.1:p.Ser1054= |