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.
Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.45329413A>C , CM000663.2:g.45329413A>C | GRCh38 |
| NC_000001.10:g.45795085A>C , CM000663.1:g.45795085A>C | GRCh37 |
| NC_000001.9:g.45567672A>C | NCBI36 |
| NG_008189.1:g.16058T>G , LRG_220:g.16058T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000412971.6:c.1075T>G | ENSP00000410263.2:p.Ser359Ala | |
| ENST00000435155.2:c.1492T>G | ENSP00000403655.2:p.Ser498Ala | |
| ENST00000467459.6:c.*321T>G | ENSP00000435889.2:n.*321T>G | |
| ENST00000483127.2:c.1477T>G | ENSP00000436469.2:p.Ser493Ala | |
| ENST00000485271.6:c.*202T>G | ENSP00000431264.2:n.*202T>G | |
| ENST00000529892.6:c.1312T>G | ENSP00000432528.2:p.Ser438Ala | |
| ENST00000533178.6:c.*788T>G | ENSP00000436430.2:n.*788T>G | |
| ENST00000672314.2:c.1459T>G | ENSP00000500828.2:p.Ser487Ala | |
| ENST00000710952.2:c.1543T>G MANE Plus Clinical | ENSP00000518552.2:p.Ser515Ala | |
| ENST00000672818.3:c.1534T>G | ENSP00000500891.1:p.Ser512Ala | |
| ENST00000456914.7:c.1459T>G MANE Select | ENSP00000407590.2:p.Ser487Ala | |
| ENST00000671898.1:c.*202T>G | ENSP00000499896.1:n.*202T>G | |
| ENST00000672011.1:c.*788T>G | ENSP00000500418.1:n.*788T>G | |
| ENST00000672818.2:c.1534T>G | ENSP00000500891.1:p.Ser512Ala | |
| ENST00000354383.10:c.1462T>G | ENSP00000346354.6:p.Ser488Ala | |
| ENST00000355498.6:c.1459T>G | ENSP00000347685.2:p.Ser487Ala | |
| ENST00000372098.7:c.1534T>G | ENSP00000361170.3:p.Ser512Ala | |
| ENST00000372104.5:c.1459T>G | ENSP00000361176.1:p.Ser487Ala | |
| ENST00000372110.7:c.1504T>G | ENSP00000361182.3:p.Ser502Ala | |
| ENST00000372115.7:c.1501T>G | ENSP00000361187.3:p.Ser501Ala | |
| ENST00000448481.5:c.1492T>G | ENSP00000409718.1:p.Ser498Ala | |
| ENST00000450313.5:c.1543T>G | ENSP00000408176.1:p.Ser515Ala | |
| ENST00000456914.6:c.1459T>G | ENSP00000407590.2:p.Ser487Ala | |
| ENST00000467459.5:c.876T>G | ENSP00000435889.1:n.876T>G | |
| ENST00000475516.5:c.*1272T>G | ENSP00000433843.1:n.*1272T>G | |
| ENST00000481571.5:c.*1272T>G | ENSP00000436597.1:n.*1272T>G | |
| ENST00000482094.5:n.780T>G | ||
| ENST00000485271.5:c.336T>G | ||
| ENST00000488731.6:c.544T>G | ENSP00000432330.1:p.Ser182Ala | |
| ENST00000528013.6:c.1501T>G | ENSP00000433130.2:p.Ser501Ala | |
| ENST00000529892.5:c.534T>G | ||
| ENST00000529984.5:c.544T>G | ENSP00000437093.1:p.Ser182Ala | |
| ENST00000531105.5:c.140T>G | ENSP00000431292.1:p.Leu47Arg | |
| ENST00000533178.5:c.1088T>G | ENSP00000436430.1:n.1088T>G | |
| NM_001048171.1:c.1501T>G | NP_001041636.1:p.Ser501Ala | |
| NM_001048172.1:c.1462T>G | NP_001041637.1:p.Ser488Ala | |
| NM_001048173.1:c.1459T>G | NP_001041638.1:p.Ser487Ala | |
| NM_001048174.1:c.1459T>G | NP_001041639.1:p.Ser487Ala | |
| NM_001128425.1:c.1543T>G , LRG_220t1:c.1543T>G | NP_001121897.1:p.Ser515Ala | |
| NM_001293190.1:c.1504T>G | NP_001280119.1:p.Ser502Ala | |
| NM_001293191.1:c.1492T>G | NP_001280120.1:p.Ser498Ala | |
| NM_001293192.1:c.1183T>G | NP_001280121.1:p.Ser395Ala | |
| NM_001293195.1:c.1459T>G | NP_001280124.1:p.Ser487Ala | |
| NM_001293196.1:c.1183T>G | NP_001280125.1:p.Ser395Ala | |
| NM_012222.2:c.1534T>G | NP_036354.1:p.Ser512Ala | |
| XM_011541497.1:c.1519T>G | XP_011539799.1:p.Ser507Ala | |
| XM_011541498.1:c.1501T>G | XP_011539800.1:p.Ser501Ala | |
| XM_011541499.1:c.1501T>G | XP_011539801.1:p.Ser501Ala | |
| XM_011541500.1:c.1501T>G | XP_011539802.1:p.Ser501Ala | |
| XM_011541501.1:c.1501T>G | XP_011539803.1:p.Ser501Ala | |
| XM_011541502.1:c.1501T>G | XP_011539804.1:p.Ser501Ala | |
| XM_011541503.1:c.1501T>G | XP_011539805.1:p.Ser501Ala | |
| XM_011541504.1:c.1492T>G | XP_011539806.1:p.Ser498Ala | |
| XM_011541505.1:c.1081T>G | XP_011539807.1:p.Ser361Ala | |
| XM_011541506.1:c.1081T>G | XP_011539808.1:p.Ser361Ala | |
| XM_011541507.1:c.1072T>G | XP_011539809.1:p.Ser358Ala | |
| XM_011541508.1:c.1087T>G | XP_011539810.1:p.Ser363Ala | |
| XR_946658.1:n.1770T>G | ||
| NM_001350650.1:c.1114T>G | NP_001337579.1:p.Ser372Ala | |
| NM_001350651.1:c.1114T>G | NP_001337580.1:p.Ser372Ala | |
| NR_146882.1:n.1897T>G | ||
| NR_146883.1:n.1711T>G | ||
| XM_011541497.3:c.1519T>G | XP_011539799.1:p.Ser507Ala | |
| XM_011541500.3:c.1501T>G | XP_011539802.1:p.Ser501Ala | |
| XM_011541501.2:c.1501T>G | XP_011539803.1:p.Ser501Ala | |
| XM_011541502.2:c.1501T>G | XP_011539804.1:p.Ser501Ala | |
| XM_011541503.2:c.1501T>G | XP_011539805.1:p.Ser501Ala | |
| XM_011541504.2:c.1492T>G | XP_011539806.1:p.Ser498Ala | |
| XM_011541505.2:c.1081T>G | XP_011539807.1:p.Ser361Ala | |
| XM_011541506.2:c.1081T>G | XP_011539808.1:p.Ser361Ala | |
| XM_017001331.1:c.1501T>G | XP_016856820.1:p.Ser501Ala | |
| XM_017001332.1:c.1501T>G | XP_016856821.1:p.Ser501Ala | |
| XM_017001333.1:c.1501T>G | XP_016856822.1:p.Ser501Ala | |
| XM_017001334.1:c.1462T>G | XP_016856823.1:p.Ser488Ala | |
| XM_017001335.1:c.1183T>G | XP_016856824.1:p.Ser395Ala | |
| XM_017001336.1:c.1114T>G | XP_016856825.1:p.Ser372Ala | |
| XM_017001337.1:c.1114T>G | XP_016856826.1:p.Ser372Ala | |
| XM_024447244.1:c.1114T>G | XP_024303012.1:p.Ser372Ala | |
| XM_024447245.1:c.1114T>G | XP_024303013.1:p.Ser372Ala | |
| XM_024447248.1:c.1072T>G | XP_024303016.1:p.Ser358Ala | |
| XM_024447249.1:c.943T>G | XP_024303017.1:p.Ser315Ala | |
| XM_024447250.1:c.943T>G | XP_024303018.1:p.Ser315Ala | |
| XM_024447251.1:c.943T>G | XP_024303019.1:p.Ser315Ala | |
| XR_001737190.1:n.1684T>G | ||
| XR_001737192.1:n.1496T>G | ||
| XR_002956643.1:n.1676T>G | ||
| XR_002956644.1:n.2211T>G | ||
| XR_946658.2:n.1784T>G | ||
| NM_001048171.2:c.1459T>G | NP_001041636.2:p.Ser487Ala | |
| NM_001128425.2:c.1543T>G MANE Plus Clinical | NP_001121897.1:p.Ser515Ala | |
| NM_001048172.2:c.1462T>G | NP_001041637.1:p.Ser488Ala | |
| NM_001048173.2:c.1459T>G | NP_001041638.1:p.Ser487Ala | |
| NM_001048174.2:c.1459T>G MANE Select | NP_001041639.1:p.Ser487Ala | |
| NM_001293190.2:c.1504T>G | NP_001280119.1:p.Ser502Ala | |
| NM_001293191.2:c.1492T>G | NP_001280120.1:p.Ser498Ala | |
| NM_001293192.2:c.1183T>G | NP_001280121.1:p.Ser395Ala | |
| NM_001293195.2:c.1459T>G | NP_001280124.1:p.Ser487Ala | |
| NM_001293196.2:c.1183T>G | NP_001280125.1:p.Ser395Ala | |
| NM_001350650.2:c.1114T>G | NP_001337579.1:p.Ser372Ala | |
| NM_001350651.2:c.1114T>G | NP_001337580.1:p.Ser372Ala | |
| NM_012222.3:c.1534T>G | NP_036354.1:p.Ser512Ala | |
| NR_146882.2:n.1867T>G | ||
| NR_146883.2:n.1716T>G |