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
ClinVar Variation Id:
365282
dbSNP Id:
rs756303645
ExAC:
9:134397475 G / A
gnomAD v2:
9-134397475-G-A
gnomAD v3:
9-131522088-G-A
gnomAD v4:
9-131522088-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131522088G>A , CM000671.2:g.131522088G>A | GRCh38 |
| NC_000009.11:g.134397475G>A , CM000671.1:g.134397475G>A | GRCh37 |
| NC_000009.10:g.133387296G>A | NCBI36 |
| NG_008896.1:g.24187G>A | |
| NG_008896.2:g.24187G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000341012.13:c.1705G>A | ENSP00000343034.7:p.Gly569Ser | |
| ENST00000404875.7:n.2407G>A | ||
| ENST00000423007.6:c.1924G>A | ENSP00000404119.2:p.Gly642Ser | |
| ENST00000677295.2:c.*2211G>A | ENSP00000504346.2:n.*2211G>A | |
| ENST00000678264.2:c.*2050G>A | ENSP00000503157.2:n.*2050G>A | |
| ENST00000682070.1:n.2291-114G>A | ||
| ENST00000682813.1:n.2271G>A | ||
| ENST00000683392.1:n.4573-114G>A | ||
| ENST00000683712.1:n.2272G>A | ||
| ENST00000683900.1:n.3767G>A | ||
| ENST00000684062.1:n.2533G>A | ||
| ENST00000684579.1:n.3713G>A | ||
| ENST00000684679.1:n.1094G>A | ||
| ENST00000341012.12:c.1705G>A | ENSP00000343034.7:p.Gly569Ser | |
| ENST00000372220.5:c.736G>A | ENSP00000361294.5:p.Gly246Ser | |
| ENST00000372228.9:c.1933G>A | ENSP00000361302.3:p.Gly645Ser | |
| ENST00000402686.8:c.1867G>A MANE Select | ENSP00000385797.4:p.Gly623Ser | |
| ENST00000676640.1:c.1867G>A | ENSP00000503281.1:p.Gly623Ser | |
| ENST00000676803.1:c.928G>A | ENSP00000503093.1:p.Gly310Ser | |
| ENST00000676835.1:c.*1082G>A | ENSP00000502911.1:n.*1082G>A | |
| ENST00000677029.1:c.1411G>A | ENSP00000502936.1:p.Gly471Ser | |
| ENST00000677099.1:c.*1577G>A | ENSP00000504553.1:n.*1577G>A | |
| ENST00000677216.1:c.1516G>A | ENSP00000503772.1:p.Gly506Ser | |
| ENST00000677221.1:n.892G>A | ||
| ENST00000677295.1:c.*1203-114G>A | ENSP00000504346.1:n.*1203-114G>A | |
| ENST00000677444.1:c.1812G>A | ||
| ENST00000677586.1:n.1234G>A | ||
| ENST00000677626.1:c.1516G>A | ENSP00000503552.1:p.Gly506Ser | |
| ENST00000677853.1:c.*875G>A | ENSP00000503488.1:n.*875G>A | |
| ENST00000678202.1:n.1026G>A | ||
| ENST00000678264.1:c.*1244G>A | ENSP00000503157.1:n.*1244G>A | |
| ENST00000678303.1:c.1777G>A | ENSP00000503696.1:p.Gly593Ser | |
| ENST00000678366.1:c.*2116G>A | ENSP00000504353.1:n.*2116G>A | |
| ENST00000678546.1:c.*1812G>A | ENSP00000503062.1:n.*1812G>A | |
| ENST00000678548.1:c.*2006G>A | ENSP00000503934.1:n.*2006G>A | |
| ENST00000678626.1:n.1703G>A | ||
| ENST00000678739.1:c.*2147-114G>A | ENSP00000503806.1:n.*2147-114G>A | |
| ENST00000678833.1:c.*1619G>A | ENSP00000503893.1:n.*1619G>A | |
| ENST00000679023.1:c.1705G>A | ENSP00000503718.1:p.Gly569Ser | |
| ENST00000679076.1:c.1486G>A | ||
| ENST00000679111.1:c.*623G>A | ENSP00000504257.1:n.*623G>A | |
| ENST00000679189.1:c.1516G>A | ENSP00000503356.1:p.Gly506Ser | |
| ENST00000341012.11:c.1705G>A | ENSP00000343034.7:p.Gly569Ser | |
| ENST00000372220.4:c.730G>A | ENSP00000361294.4:p.Gly244Ser | |
| ENST00000372228.7:c.1933G>A | ENSP00000361302.3:p.Gly645Ser | |
| ENST00000402686.7:c.1867G>A | ENSP00000385797.3:p.Gly623Ser | |
| ENST00000404875.6:c.1516G>A | ENSP00000384531.2:p.Gly506Ser | |
| ENST00000423007.5:c.1867G>A | ENSP00000404119.1:p.Gly623Ser | |
| ENST00000485278.5:n.2417G>A | ||
| ENST00000494883.1:n.410G>A | ||
| NM_001077365.1:c.1867G>A | NP_001070833.1:p.Gly623Ser | |
| NM_001077366.1:c.1705G>A | NP_001070834.1:p.Gly569Ser | |
| NM_001136113.1:c.1867G>A | NP_001129585.1:p.Gly623Ser | |
| NM_001136114.1:c.1516G>A | NP_001129586.1:p.Gly506Ser | |
| NM_007171.3:c.1933G>A | NP_009102.3:p.Gly645Ser | |
| XM_005272156.1:c.1933G>A | XP_005272213.1:p.Gly645Ser | |
| XM_005272158.1:c.1771G>A | XP_005272215.1:p.Gly591Ser | |
| XM_005272159.1:c.1582G>A | XP_005272216.1:p.Gly528Ser | |
| XM_005272162.1:c.736G>A | XP_005272219.1:p.Gly246Ser | |
| XM_006716932.1:c.1582G>A | XP_006716995.1:p.Gly528Ser | |
| XM_011518140.1:c.1786G>A | XP_011516442.1:p.Gly596Ser | |
| XM_011518141.1:c.1720G>A | XP_011516443.1:p.Gly574Ser | |
| XM_011518142.1:c.1624G>A | XP_011516444.1:p.Gly542Ser | |
| XM_011518143.1:c.1618G>A | XP_011516445.1:p.Gly540Ser | |
| XM_011518145.1:c.1477G>A | XP_011516447.1:p.Gly493Ser | |
| XM_011518147.1:c.805G>A | XP_011516449.1:p.Gly269Ser | |
| XR_929703.1:n.2109G>A | ||
| NM_001353193.1:c.1933G>A | NP_001340122.1:p.Gly645Ser | |
| NM_001353194.1:c.1705G>A | NP_001340123.1:p.Gly569Ser | |
| NM_001353195.1:c.1516G>A | NP_001340124.1:p.Gly506Ser | |
| NM_001353196.1:c.1777G>A | NP_001340125.1:p.Gly593Ser | |
| NM_001353197.1:c.1771G>A | NP_001340126.1:p.Gly591Ser | |
| NM_001353198.1:c.1771G>A | NP_001340127.1:p.Gly591Ser | |
| NM_001353199.1:c.1582G>A | NP_001340128.1:p.Gly528Ser | |
| NM_001353200.1:c.1411G>A | NP_001340129.1:p.Gly471Ser | |
| NR_148391.1:n.1917G>A | ||
| NR_148392.1:n.2135G>A | ||
| NR_148393.1:n.2056G>A | ||
| NR_148394.1:n.1810G>A | ||
| NR_148395.1:n.2208G>A | ||
| NR_148396.1:n.1842G>A | ||
| NR_148397.1:n.1967G>A | ||
| NR_148398.1:n.1922G>A | ||
| NR_148399.1:n.2448G>A | ||
| NR_148400.1:n.2047G>A | ||
| XM_005272162.3:c.736G>A | XP_005272219.1:p.Gly246Ser | |
| XM_006716932.2:c.1582G>A | XP_006716995.1:p.Gly528Ser | |
| XM_011518140.2:c.1786G>A | XP_011516442.1:p.Gly596Ser | |
| XM_011518141.2:c.1720G>A | XP_011516443.1:p.Gly574Ser | |
| XM_011518142.2:c.1624G>A | XP_011516444.1:p.Gly542Ser | |
| XM_011518143.2:c.1618G>A | XP_011516445.1:p.Gly540Ser | |
| XM_011518145.2:c.1477G>A | XP_011516447.1:p.Gly493Ser | |
| XM_017014205.2:c.736G>A | XP_016869694.1:p.Gly246Ser | |
| XM_024447380.1:c.736G>A | XP_024303148.1:p.Gly246Ser | |
| XM_024447381.1:c.1042G>A | XP_024303149.1:p.Gly348Ser | |
| XM_024447382.1:c.736G>A | XP_024303150.1:p.Gly246Ser | |
| XR_001746160.2:n.2037G>A | ||
| XR_001746162.2:n.2242G>A | ||
| XR_001746164.1:n.1959G>A | ||
| XR_001746166.2:n.2254G>A | ||
| NM_001077365.2:c.1867G>A MANE Select | NP_001070833.1:p.Gly623Ser | |
| NM_001077366.2:c.1705G>A | NP_001070834.1:p.Gly569Ser | |
| NM_001136113.2:c.1867G>A | NP_001129585.1:p.Gly623Ser | |
| NM_001136114.2:c.1516G>A | NP_001129586.1:p.Gly506Ser | |
| NM_001353193.2:c.1933G>A | NP_001340122.2:p.Gly645Ser | |
| NM_001353194.2:c.1705G>A | NP_001340123.1:p.Gly569Ser | |
| NM_001353195.2:c.1516G>A | NP_001340124.1:p.Gly506Ser | |
| NM_001353196.2:c.1777G>A | NP_001340125.1:p.Gly593Ser | |
| NM_001353197.2:c.1771G>A | NP_001340126.2:p.Gly591Ser | |
| NM_001353198.2:c.1771G>A | NP_001340127.2:p.Gly591Ser | |
| NM_001353199.2:c.1582G>A | NP_001340128.2:p.Gly528Ser | |
| NM_001353200.2:c.1411G>A | NP_001340129.1:p.Gly471Ser | |
| NM_001374689.1:c.1855G>A | NP_001361618.1:p.Gly619Ser | |
| NM_001374690.1:c.1648G>A | NP_001361619.1:p.Gly550Ser | |
| NM_001374691.1:c.1516G>A | NP_001361620.1:p.Gly506Ser | |
| NM_001374692.1:c.1516G>A | NP_001361621.1:p.Gly506Ser | |
| NM_001374693.1:c.1516G>A | NP_001361622.1:p.Gly506Ser | |
| NM_001374695.1:c.1477G>A | NP_001361624.1:p.Gly493Ser | |
| NM_007171.4:c.1933G>A | NP_009102.4:p.Gly645Ser | |
| NR_148391.2:n.1901G>A | ||
| NR_148392.2:n.2119G>A | ||
| NR_148393.2:n.2040G>A | ||
| NR_148394.2:n.1794G>A | ||
| NR_148395.2:n.2192G>A | ||
| NR_148396.2:n.1826G>A | ||
| NR_148397.2:n.1951G>A | ||
| NR_148398.2:n.1906G>A | ||
| NR_148399.2:n.2432G>A | ||
| NR_148400.2:n.2031G>A |