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.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.50055016A>C , CM000664.2:g.50055016A>C | GRCh38 |
| NC_000002.11:g.50282154A>C , CM000664.1:g.50282154A>C | GRCh37 |
| NC_000002.10:g.50135658A>C | NCBI36 |
| NG_011878.1:g.982521T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000401669.7:c.3747T>G MANE Select | ENSP00000385017.2:p.Ile1249Met | |
| ENST00000637889.1:n.914T>G | ||
| ENST00000637906.1:c.606-1426T>G | ENSP00000490198.1:n.606-1426T>G | |
| ENST00000342183.9:c.614-1426T>G | ENSP00000341184.5:n.614-1426T>G | |
| ENST00000401669.6:c.3747T>G | ENSP00000385017.2:p.Ile1249Met | |
| ENST00000401710.5:c.642T>G | ENSP00000385580.2:p.Ile214Met | |
| ENST00000404971.5:c.3867T>G | ENSP00000385142.1:p.Ile1289Met | |
| ENST00000405472.7:c.3711T>G | ENSP00000434015.2:p.Ile1237Met | |
| ENST00000406316.6:c.3719-1426T>G | ENSP00000384311.2:n.3719-1426T>G | |
| ENST00000611589.4:c.-119-1426T>G | ENSP00000483634.1:n.-119-1426T>G | |
| ENST00000625672.2:c.3723T>G | ENSP00000485887.1:p.Ile1241Met | |
| ENST00000628364.2:c.642T>G | ENSP00000485815.1:p.Ile214Met | |
| ENST00000630543.2:c.3723T>G | ENSP00000486879.1:p.Ile1241Met | |
| ENST00000635264.1:n.556T>G | ||
| NM_001135659.1:c.3867T>G | NP_001129131.1:p.Ile1289Met | |
| NM_004801.4:c.3719-1426T>G | NP_004792.1:n.3719-1426T>G | |
| NM_138735.2:c.614-1426T>G | NP_620072.1:n.614-1426T>G | |
| XM_005264642.2:c.3768T>G | XP_005264699.1:p.Ile1256Met | |
| XM_005264643.2:c.3723T>G | XP_005264700.1:p.Ile1241Met | |
| XM_006712137.2:c.3740-1426T>G | XP_006712200.1:n.3740-1426T>G | |
| XM_006712140.2:c.3768T>G | XP_006712203.1:p.Ile1256Met | |
| XM_011533167.1:c.3768T>G | XP_011531469.1:p.Ile1256Met | |
| XM_011533168.1:c.3765T>G | XP_011531470.1:p.Ile1255Met | |
| XM_011533169.1:c.3756T>G | XP_011531471.1:p.Ile1252Met | |
| XM_011533170.1:c.3750T>G | XP_011531472.1:p.Ile1250Met | |
| XM_011533171.1:c.3747T>G | XP_011531473.1:p.Ile1249Met | |
| XM_011533172.1:c.3741T>G | XP_011531474.1:p.Ile1247Met | |
| XM_011533173.1:c.3738T>G | XP_011531475.1:p.Ile1246Met | |
| XM_011533174.1:c.3723T>G | XP_011531476.1:p.Ile1241Met | |
| XM_011533175.1:c.3711T>G | XP_011531477.1:p.Ile1237Met | |
| XM_011533176.1:c.3708T>G | XP_011531478.1:p.Ile1236Met | |
| XM_011533177.1:c.3740-1426T>G | XP_011531479.1:n.3740-1426T>G | |
| XM_011533178.1:c.3678T>G | XP_011531480.1:p.Ile1226Met | |
| XM_011533179.1:c.3695-1426T>G | XP_011531481.1:n.3695-1426T>G | |
| XM_011533180.1:c.3768T>G | XP_011531482.1:p.Ile1256Met | |
| XM_011533181.1:c.2973T>G | XP_011531483.1:p.Ile991Met | |
| XM_011533182.1:c.2928T>G | XP_011531484.1:p.Ile976Met | |
| XM_011533183.1:c.2901T>G | XP_011531485.1:p.Ile967Met | |
| XM_011533184.1:c.2808T>G | XP_011531486.1:p.Ile936Met | |
| NM_001135659.2:c.3867T>G | NP_001129131.1:p.Ile1289Met | |
| NM_001330077.1:c.3723T>G | NP_001317006.1:p.Ile1241Met | |
| NM_001330078.1:c.3747T>G | NP_001317007.1:p.Ile1249Met | |
| NM_001330082.1:c.3723T>G | NP_001317011.1:p.Ile1241Met | |
| NM_001330083.1:c.3653-1426T>G | NP_001317012.1:n.3653-1426T>G | |
| NM_001330084.1:c.3681T>G | NP_001317013.1:p.Ile1227Met | |
| NM_001330085.1:c.3720T>G | NP_001317014.1:p.Ile1240Met | |
| NM_001330086.1:c.3747T>G | NP_001317015.1:p.Ile1249Met | |
| NM_001330087.1:c.3608-1426T>G | NP_001317016.1:n.3608-1426T>G | |
| NM_001330088.1:c.3638-1426T>G | NP_001317017.1:n.3638-1426T>G | |
| NM_001330091.1:c.642T>G | NP_001317020.1:p.Ile214Met | |
| NM_001330092.1:c.642T>G | NP_001317021.1:p.Ile214Met | |
| NM_001330093.1:c.3744T>G | NP_001317022.1:p.Ile1248Met | |
| NM_001330094.1:c.3735T>G | NP_001317023.1:p.Ile1245Met | |
| NM_001330095.1:c.3668-1426T>G | NP_001317024.1:n.3668-1426T>G | |
| NM_001330096.1:c.3608-1426T>G | NP_001317025.1:n.3608-1426T>G | |
| NM_001330097.1:c.614-1426T>G | NP_001317026.1:n.614-1426T>G | |
| NM_004801.5:c.3719-1426T>G | NP_004792.1:n.3719-1426T>G | |
| NM_138735.4:c.614-1426T>G | NP_620072.1:n.614-1426T>G | |
| XM_005264642.4:c.3768T>G | XP_005264699.1:p.Ile1256Met | |
| XM_006712137.4:c.3740-1426T>G | XP_006712200.1:n.3740-1426T>G | |
| XM_006712140.4:c.3795T>G | XP_006712203.2:p.Ile1265Met | |
| XM_011533167.3:c.3768T>G | XP_011531469.1:p.Ile1256Met | |
| XM_011533172.3:c.3741T>G | XP_011531474.1:p.Ile1247Met | |
| XM_011533175.3:c.3711T>G | XP_011531477.1:p.Ile1237Met | |
| XM_011533177.3:c.3740-1426T>G | XP_011531479.1:n.3740-1426T>G | |
| XM_011533178.3:c.3678T>G | XP_011531480.1:p.Ile1226Met | |
| XM_011533180.3:c.3768T>G | XP_011531482.1:p.Ile1256Met | |
| XM_011533183.2:c.2901T>G | XP_011531485.1:p.Ile967Met | |
| XM_017005303.2:c.3795T>G | XP_016860792.1:p.Ile1265Met | |
| XM_017005304.2:c.3792T>G | XP_016860793.1:p.Ile1264Met | |
| XM_017005305.2:c.3795T>G | XP_016860794.1:p.Ile1265Met | |
| XM_017005306.2:c.3783T>G | XP_016860795.1:p.Ile1261Met | |
| XM_017005307.2:c.3777T>G | XP_016860796.1:p.Ile1259Met | |
| XM_017005308.2:c.3774T>G | XP_016860797.1:p.Ile1258Met | |
| XM_017005309.2:c.3768T>G | XP_016860798.1:p.Ile1256Met | |
| XM_017005310.2:c.3765T>G | XP_016860799.1:p.Ile1255Met | |
| XM_017005311.2:c.3750T>G | XP_016860800.1:p.Ile1250Met | |
| XM_017005314.2:c.3735T>G | XP_016860803.1:p.Ile1245Met | |
| XM_017005315.2:c.3741T>G | XP_016860804.1:p.Ile1247Met | |
| XM_017005316.2:c.3732T>G | XP_016860805.1:p.Ile1244Met | |
| XM_017005318.2:c.3723T>G | XP_016860807.1:p.Ile1241Met | |
| XM_017005320.2:c.3720T>G | XP_016860809.1:p.Ile1240Met | |
| XM_017005321.2:c.3767-1426T>G | XP_016860810.1:n.3767-1426T>G | |
| XM_017005322.2:c.3767-1426T>G | XP_016860811.1:n.3767-1426T>G | |
| XM_017005324.2:c.3713-1426T>G | XP_016860813.1:n.3713-1426T>G | |
| XM_017005325.2:c.3713-1426T>G | XP_016860814.1:n.3713-1426T>G | |
| XM_017005326.2:c.3701-1426T>G | XP_016860815.1:n.3701-1426T>G | |
| XM_017005327.2:c.3695-1426T>G | XP_016860816.1:n.3695-1426T>G | |
| XM_017005329.2:c.3795T>G | XP_016860818.1:p.Ile1265Met | |
| XM_017005334.2:c.2835T>G | XP_016860823.1:p.Ile945Met | |
| NM_001330078.2:c.3747T>G MANE Select | NP_001317007.1:p.Ile1249Met | |
| NM_001135659.3:c.3867T>G | NP_001129131.1:p.Ile1289Met | |
| NM_001330077.2:c.3723T>G | NP_001317006.1:p.Ile1241Met | |
| NM_001330082.2:c.3723T>G | NP_001317011.1:p.Ile1241Met | |
| NM_001330083.2:c.3653-1426T>G | NP_001317012.1:n.3653-1426T>G | |
| NM_001330084.2:c.3681T>G | NP_001317013.1:p.Ile1227Met | |
| NM_001330085.2:c.3720T>G | NP_001317014.1:p.Ile1240Met | |
| NM_001330086.2:c.3747T>G | NP_001317015.1:p.Ile1249Met | |
| NM_001330087.2:c.3608-1426T>G | NP_001317016.1:n.3608-1426T>G | |
| NM_001330088.2:c.3638-1426T>G | NP_001317017.1:n.3638-1426T>G | |
| NM_001330091.2:c.642T>G | NP_001317020.1:p.Ile214Met | |
| NM_001330092.2:c.642T>G | NP_001317021.1:p.Ile214Met | |
| NM_001330093.2:c.3744T>G | NP_001317022.1:p.Ile1248Met | |
| NM_001330094.2:c.3735T>G | NP_001317023.1:p.Ile1245Met | |
| NM_001330095.2:c.3668-1426T>G | NP_001317024.1:n.3668-1426T>G | |
| NM_001330096.2:c.3608-1426T>G | NP_001317025.1:n.3608-1426T>G | |
| NM_001330097.2:c.614-1426T>G | NP_001317026.1:n.614-1426T>G | |
| NM_004801.6:c.3719-1426T>G | NP_004792.1:n.3719-1426T>G | |
| NM_138735.5:c.614-1426T>G | NP_620072.1:n.614-1426T>G |