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_000016.10:g.2084240T>G , CM000678.2:g.2084240T>G | GRCh38 |
| NC_000016.9:g.2134241T>G , CM000678.1:g.2134241T>G | GRCh37 |
| NC_000016.8:g.2074242T>G | NCBI36 |
| NG_005895.1:g.39935T>G , LRG_487:g.39935T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*2367T>G | ENSP00000455997.2:n.*2367T>G | |
| ENST00000642206.2:c.3865T>G | ENSP00000495146.2:p.Ser1289Ala | |
| ENST00000642365.2:c.4015T>G | ENSP00000495459.2:p.Ser1339Ala | |
| ENST00000644417.2:c.*4398T>G | ENSP00000493912.2:n.*4398T>G | |
| ENST00000646464.2:c.*6767T>G | ENSP00000496610.2:n.*6767T>G | |
| ENST00000219476.9:c.4018T>G MANE Select | ENSP00000219476.3:p.Ser1340Ala | |
| ENST00000350773.9:c.3949T>G | ENSP00000344383.4:p.Ser1317Ala | |
| ENST00000401874.7:c.3817T>G | ENSP00000384468.2:p.Ser1273Ala | |
| ENST00000568454.6:c.3850T>G | ENSP00000454487.1:p.Ser1284Ala | |
| ENST00000569110.2:c.254T>G | ||
| ENST00000569930.2:n.1900T>G | ||
| ENST00000642365.1:c.2672T>G | ||
| ENST00000642561.1:c.3889T>G | ENSP00000495099.1:p.Ser1297Ala | |
| ENST00000642728.1:n.200T>G | ||
| ENST00000642797.1:c.3820T>G | ENSP00000493846.1:p.Ser1274Ala | |
| ENST00000642936.1:c.3886T>G | ENSP00000494514.1:p.Ser1296Ala | |
| ENST00000643088.1:c.3817T>G | ENSP00000494747.1:p.Ser1273Ala | |
| ENST00000643177.1:n.32T>G | ||
| ENST00000643426.1:n.1666T>G | ||
| ENST00000643533.1:n.459T>G | ||
| ENST00000643946.1:c.3949T>G | ENSP00000495927.1:p.Ser1317Ala | |
| ENST00000644043.1:c.3889T>G | ENSP00000496262.1:p.Ser1297Ala | |
| ENST00000644329.1:c.3817T>G | ENSP00000496611.1:p.Ser1273Ala | |
| ENST00000644335.1:c.3820T>G | ENSP00000496317.1:p.Ser1274Ala | |
| ENST00000644399.1:c.3939T>G | ||
| ENST00000645024.1:n.2102T>G | ||
| ENST00000645186.1:c.261T>G | ||
| ENST00000646388.1:c.4018T>G | ENSP00000495921.1:p.Ser1340Ala | |
| ENST00000646634.1:n.2833T>G | ||
| ENST00000646674.1:n.1270T>G | ||
| ENST00000647042.1:n.1241T>G | ||
| ENST00000647180.1:n.1131T>G | ||
| ENST00000219476.7:c.4018T>G | ENSP00000219476.3:p.Ser1340Ala | |
| ENST00000350773.8:c.3949T>G | ENSP00000344383.4:p.Ser1317Ala | |
| ENST00000382538.10:c.3673T>G | ENSP00000371978.6:p.Ser1225Ala | |
| ENST00000401874.6:c.3817T>G | ENSP00000384468.2:p.Ser1273Ala | |
| ENST00000439117.6:c.*3185T>G | ENSP00000406980.2:n.*3185T>G | |
| ENST00000439673.6:c.3709T>G | ENSP00000399232.2:p.Ser1237Ala | |
| ENST00000497886.5:n.1776T>G | ||
| ENST00000568454.5:c.3850T>G | ENSP00000454487.1:p.Ser1284Ala | |
| ENST00000569110.1:c.200T>G | ||
| ENST00000569930.1:n.1133T>G | ||
| NM_000548.3:c.4018T>G , LRG_487t1:c.4018T>G | NP_000539.2:p.Ser1340Ala | |
| NM_001077183.1:c.3817T>G | NP_001070651.1:p.Ser1273Ala | |
| NM_001114382.1:c.3949T>G | NP_001107854.1:p.Ser1317Ala | |
| XM_005255529.3:c.3889T>G | XP_005255586.2:p.Ser1297Ala | |
| XM_005255531.3:c.3820T>G | XP_005255588.2:p.Ser1274Ala | |
| XM_011522636.1:c.4072T>G | XP_011520938.1:p.Ser1358Ala | |
| XM_011522637.1:c.4069T>G | XP_011520939.1:p.Ser1357Ala | |
| XM_011522638.1:c.3961T>G | XP_011520940.1:p.Ser1321Ala | |
| XM_011522639.1:c.3943T>G | XP_011520941.1:p.Ser1315Ala | |
| XM_011522640.1:c.3940T>G | XP_011520942.1:p.Ser1314Ala | |
| XM_011522641.1:c.3709T>G | XP_011520943.1:p.Ser1237Ala | |
| NM_000548.4:c.4018T>G | NP_000539.2:p.Ser1340Ala | |
| NM_001077183.2:c.3817T>G | NP_001070651.1:p.Ser1273Ala | |
| NM_001114382.2:c.3949T>G | NP_001107854.1:p.Ser1317Ala | |
| NM_001318827.1:c.3709T>G | NP_001305756.1:p.Ser1237Ala | |
| NM_001318829.1:c.3673T>G | NP_001305758.1:p.Ser1225Ala | |
| NM_001318831.1:c.3286T>G | NP_001305760.1:p.Ser1096Ala | |
| NM_001318832.1:c.3850T>G | NP_001305761.1:p.Ser1284Ala | |
| NM_001363528.1:c.3820T>G | NP_001350457.1:p.Ser1274Ala | |
| NM_021055.2:c.3889T>G | NP_066399.2:p.Ser1297Ala | |
| XM_005255531.4:c.3820T>G | XP_005255588.2:p.Ser1274Ala | |
| XM_011522636.2:c.4072T>G | XP_011520938.1:p.Ser1358Ala | |
| XM_011522637.2:c.4069T>G | XP_011520939.1:p.Ser1357Ala | |
| XM_011522638.2:c.4234T>G | XP_011520940.2:p.Ser1412Ala | |
| XM_011522639.2:c.3943T>G | XP_011520941.1:p.Ser1315Ala | |
| XM_011522640.2:c.3940T>G | XP_011520942.1:p.Ser1314Ala | |
| XM_017023615.1:c.4015T>G | XP_016879104.1:p.Ser1339Ala | |
| XM_017023616.1:c.3886T>G | XP_016879105.1:p.Ser1296Ala | |
| XM_017023617.1:c.3982T>G | XP_016879106.1:p.Ser1328Ala | |
| XM_017023618.1:c.2728T>G | XP_016879107.1:p.Ser910Ala | |
| XM_024450413.1:c.3817T>G | XP_024306181.1:p.Ser1273Ala | |
| NM_000548.5:c.4018T>G MANE Select | NP_000539.2:p.Ser1340Ala | |
| NM_001370404.1:c.3886T>G | NP_001357333.1:p.Ser1296Ala | |
| NM_001370405.1:c.3889T>G | NP_001357334.1:p.Ser1297Ala | |
| NM_001077183.3:c.3817T>G | NP_001070651.1:p.Ser1273Ala | |
| NM_001114382.3:c.3949T>G | NP_001107854.1:p.Ser1317Ala | |
| NM_001318827.2:c.3709T>G | NP_001305756.1:p.Ser1237Ala | |
| NM_001318829.2:c.3673T>G | NP_001305758.1:p.Ser1225Ala | |
| NM_001318831.2:c.3286T>G | NP_001305760.1:p.Ser1096Ala | |
| NM_001318832.2:c.3850T>G | NP_001305761.1:p.Ser1284Ala | |
| NM_001363528.2:c.3820T>G | NP_001350457.1:p.Ser1274Ala | |
| NM_021055.3:c.3889T>G | NP_066399.2:p.Ser1297Ala |