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_000001.11:g.45332182C= , CM000663.2:g.45332182C= | GRCh38 |
| NC_000001.10:g.45797854C= , CM000663.1:g.45797854C= | GRCh37 |
| NC_000001.9:g.45570441C= | NCBI36 |
| NG_008189.1:g.13289G= , LRG_220:g.13289G= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412971.6:c.449G= | ENSP00000410263.2:p.Cys150= | |
| ENST00000435155.2:c.866G= | ENSP00000403655.2:p.Cys289= | |
| ENST00000467459.6:c.833G= | ENSP00000435889.2:p.Cys278= | |
| ENST00000483127.2:c.851G= | ENSP00000436469.2:p.Cys284= | |
| ENST00000485271.6:c.833G= | ENSP00000431264.2:p.Cys278= | |
| ENST00000529892.6:c.875G= | ENSP00000432528.2:p.Cys292= | |
| ENST00000533178.6:c.*162G= | ENSP00000436430.2:n.*162G= | |
| ENST00000672314.2:c.833G= | ENSP00000500828.2:p.Cys278= | |
| ENST00000710952.2:c.917G= MANE Plus Clinical | ENSP00000518552.2:p.Cys306= | |
| ENST00000672818.3:c.908G= | ENSP00000500891.1:p.Cys303= | |
| ENST00000456914.7:c.833G= MANE Select | ENSP00000407590.2:p.Cys278= | |
| ENST00000461495.6:c.*572G= | ENSP00000437166.1:n.*572G= | |
| ENST00000671898.1:c.1421G= | ENSP00000499896.1:p.Cys474= | |
| ENST00000672011.1:c.*162G= | ENSP00000500418.1:n.*162G= | |
| ENST00000672314.1:c.833G= | ENSP00000500828.1:p.Cys278= | |
| ENST00000672593.1:c.*886G= | ENSP00000500455.1:n.*886G= | |
| ENST00000672764.1:c.*162G= | ENSP00000500886.1:n.*162G= | |
| ENST00000672818.2:c.908G= | ENSP00000500891.1:p.Cys303= | |
| ENST00000673134.1:c.*530G= | ENSP00000500526.1:n.*530G= | |
| ENST00000354383.10:c.836G= | ENSP00000346354.6:p.Cys279= | |
| ENST00000355498.6:c.833G= | ENSP00000347685.2:p.Cys278= | |
| ENST00000372098.7:c.908G= | ENSP00000361170.3:p.Cys303= | |
| ENST00000372104.5:c.833G= | ENSP00000361176.1:p.Cys278= | |
| ENST00000372110.7:c.878G= | ENSP00000361182.3:p.Cys293= | |
| ENST00000372115.7:c.875G= | ENSP00000361187.3:p.Cys292= | |
| ENST00000412971.5:c.449G= | ENSP00000410263.1:p.Cys150= | |
| ENST00000435155.1:c.866G= | ENSP00000403655.1:p.Cys289= | |
| ENST00000448481.5:c.866G= | ENSP00000409718.1:p.Cys289= | |
| ENST00000450313.5:c.917G= | ENSP00000408176.1:p.Cys306= | |
| ENST00000456914.6:c.833G= | ENSP00000407590.2:p.Cys278= | |
| ENST00000461495.5:c.*572G= | ENSP00000437166.1:n.*572G= | |
| ENST00000462388.5:n.524G= | ||
| ENST00000466231.1:n.198G= | ||
| ENST00000467459.5:c.227G= | ENSP00000435889.1:p.Cys76= | |
| ENST00000470256.5:c.*162G= | ENSP00000434985.1:n.*162G= | |
| ENST00000475516.5:c.*646G= | ENSP00000433843.1:n.*646G= | |
| ENST00000481571.5:c.*646G= | ENSP00000436597.1:n.*646G= | |
| ENST00000488731.6:c.187+581G= | ENSP00000432330.1:n.187+581G= | |
| ENST00000528013.6:c.875G= | ENSP00000433130.2:p.Cys292= | |
| ENST00000529892.5:c.97G= | ||
| ENST00000529984.5:c.187+581G= | ENSP00000437093.1:n.187+581G= | |
| ENST00000531105.5:c.115+2209G= | ENSP00000431292.1:n.115+2209G= | |
| ENST00000533178.5:c.462G= | ENSP00000436430.1:n.462G= | |
| NM_001048171.1:c.875G= | NP_001041636.1:p.Cys292= | |
| NM_001048172.1:c.836G= | NP_001041637.1:p.Cys279= | |
| NM_001048173.1:c.833G= | NP_001041638.1:p.Cys278= | |
| NM_001048174.1:c.833G= | NP_001041639.1:p.Cys278= | |
| NM_001128425.1:c.917G= , LRG_220t1:c.917G= | NP_001121897.1:p.Cys306= | |
| NM_001293190.1:c.878G= | NP_001280119.1:p.Cys293= | |
| NM_001293191.1:c.866G= | NP_001280120.1:p.Cys289= | |
| NM_001293192.1:c.557G= | NP_001280121.1:p.Cys186= | |
| NM_001293195.1:c.833G= | NP_001280124.1:p.Cys278= | |
| NM_001293196.1:c.557G= | NP_001280125.1:p.Cys186= | |
| NM_012222.2:c.908G= | NP_036354.1:p.Cys303= | |
| XM_011541497.1:c.893G= | XP_011539799.1:p.Cys298= | |
| XM_011541498.1:c.875G= | XP_011539800.1:p.Cys292= | |
| XM_011541499.1:c.875G= | XP_011539801.1:p.Cys292= | |
| XM_011541500.1:c.875G= | XP_011539802.1:p.Cys292= | |
| XM_011541501.1:c.875G= | XP_011539803.1:p.Cys292= | |
| XM_011541502.1:c.875G= | XP_011539804.1:p.Cys292= | |
| XM_011541503.1:c.875G= | XP_011539805.1:p.Cys292= | |
| XM_011541504.1:c.866G= | XP_011539806.1:p.Cys289= | |
| XM_011541505.1:c.455G= | XP_011539807.1:p.Cys152= | |
| XM_011541506.1:c.455G= | XP_011539808.1:p.Cys152= | |
| XM_011541507.1:c.446G= | XP_011539809.1:p.Cys149= | |
| XM_011541508.1:c.461G= | XP_011539810.1:p.Cys154= | |
| XR_946658.1:n.964G= | ||
| NM_001350650.1:c.488G= | NP_001337579.1:p.Cys163= | |
| NM_001350651.1:c.488G= | NP_001337580.1:p.Cys163= | |
| NR_146882.1:n.1091G= | ||
| NR_146883.1:n.905G= | ||
| XM_011541497.3:c.893G= | XP_011539799.1:p.Cys298= | |
| XM_011541500.3:c.875G= | XP_011539802.1:p.Cys292= | |
| XM_011541501.2:c.875G= | XP_011539803.1:p.Cys292= | |
| XM_011541502.2:c.875G= | XP_011539804.1:p.Cys292= | |
| XM_011541503.2:c.875G= | XP_011539805.1:p.Cys292= | |
| XM_011541504.2:c.866G= | XP_011539806.1:p.Cys289= | |
| XM_011541505.2:c.455G= | XP_011539807.1:p.Cys152= | |
| XM_011541506.2:c.455G= | XP_011539808.1:p.Cys152= | |
| XM_017001331.1:c.875G= | XP_016856820.1:p.Cys292= | |
| XM_017001332.1:c.875G= | XP_016856821.1:p.Cys292= | |
| XM_017001333.1:c.875G= | XP_016856822.1:p.Cys292= | |
| XM_017001334.1:c.836G= | XP_016856823.1:p.Cys279= | |
| XM_017001335.1:c.557G= | XP_016856824.1:p.Cys186= | |
| XM_017001336.1:c.488G= | XP_016856825.1:p.Cys163= | |
| XM_017001337.1:c.488G= | XP_016856826.1:p.Cys163= | |
| XM_024447244.1:c.488G= | XP_024303012.1:p.Cys163= | |
| XM_024447245.1:c.488G= | XP_024303013.1:p.Cys163= | |
| XM_024447248.1:c.446G= | XP_024303016.1:p.Cys149= | |
| XM_024447249.1:c.317G= | XP_024303017.1:p.Cys106= | |
| XM_024447250.1:c.317G= | XP_024303018.1:p.Cys106= | |
| XM_024447251.1:c.317G= | XP_024303019.1:p.Cys106= | |
| XR_001737190.1:n.878G= | ||
| XR_001737192.1:n.690G= | ||
| XR_002956643.1:n.870G= | ||
| XR_002956644.1:n.1405G= | ||
| XR_946658.2:n.978G= | ||
| NM_001048171.2:c.833G= | NP_001041636.2:p.Cys278= | |
| NM_001128425.2:c.917G= MANE Plus Clinical | NP_001121897.1:p.Cys306= | |
| NM_001048172.2:c.836G= | NP_001041637.1:p.Cys279= | |
| NM_001048173.2:c.833G= | NP_001041638.1:p.Cys278= | |
| NM_001048174.2:c.833G= MANE Select | NP_001041639.1:p.Cys278= | |
| NM_001293190.2:c.878G= | NP_001280119.1:p.Cys293= | |
| NM_001293191.2:c.866G= | NP_001280120.1:p.Cys289= | |
| NM_001293192.2:c.557G= | NP_001280121.1:p.Cys186= | |
| NM_001293195.2:c.833G= | NP_001280124.1:p.Cys278= | |
| NM_001293196.2:c.557G= | NP_001280125.1:p.Cys186= | |
| NM_001350650.2:c.488G= | NP_001337579.1:p.Cys163= | |
| NM_001350651.2:c.488G= | NP_001337580.1:p.Cys163= | |
| NM_012222.3:c.908G= | NP_036354.1:p.Cys303= | |
| NR_146882.2:n.1061G= | ||
| NR_146883.2:n.910G= |