Linked Data
ClinVar Variation Id:
39434
ClinVar RCV Id:
RCV000032629
dbSNP Id:
rs397514501
gnomAD v4:
9-131508913-A-G
PubMed:
PMID:22549409
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131508913A>G , CM000671.2:g.131508913A>G | GRCh38 |
| NC_000009.11:g.134384300A>G , CM000671.1:g.134384300A>G | GRCh37 |
| NC_000009.10:g.133374121A>G | NCBI36 |
| NG_008896.1:g.11012A>G | |
| NG_008896.2:g.11012A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341012.13:c.268A>G | ENSP00000343034.7:p.Asn90Asp | |
| ENST00000404875.7:n.539A>G | ||
| ENST00000423007.6:c.421A>G | ENSP00000404119.2:p.Asn141Asp | |
| ENST00000462375.7:n.3A>G | ||
| ENST00000677295.2:c.*506A>G | ENSP00000504346.2:n.*506A>G | |
| ENST00000678264.2:c.*613A>G | ENSP00000503157.2:n.*613A>G | |
| ENST00000678942.2:c.125A>G | ENSP00000504690.2:p.Glu42Gly | |
| ENST00000682070.1:n.627A>G | ||
| ENST00000682563.1:n.3A>G | ||
| ENST00000682813.1:n.432A>G | ||
| ENST00000683229.1:c.-27A>G | ENSP00000506964.1:n.-27A>G | |
| ENST00000683392.1:n.2914A>G | ||
| ENST00000683712.1:n.567A>G | ||
| ENST00000683900.1:n.1604-830A>G | ||
| ENST00000684062.1:n.739A>G | ||
| ENST00000684579.1:n.2008A>G | ||
| ENST00000341012.12:c.268A>G | ENSP00000343034.7:p.Asn90Asp | |
| ENST00000372220.5:c.-145-3128A>G | ENSP00000361294.5:n.-145-3128A>G | |
| ENST00000372228.9:c.430A>G | ENSP00000361302.3:p.Asn144Asp | |
| ENST00000402686.8:c.430A>G MANE Select | ENSP00000385797.4:p.Asn144Asp | |
| ENST00000415075.6:c.*140A>G | ENSP00000405149.2:n.*140A>G | |
| ENST00000430619.2:c.-27A>G | ENSP00000402083.2:n.-27A>G | |
| ENST00000462375.6:n.254A>G | ||
| ENST00000676640.1:c.430A>G | ENSP00000503281.1:p.Asn144Asp | |
| ENST00000676803.1:c.-126-1347A>G | ENSP00000503093.1:n.-126-1347A>G | |
| ENST00000676835.1:c.79A>G | ENSP00000502911.1:p.Asn27Asp | |
| ENST00000676915.1:c.283A>G | ENSP00000504628.1:p.Asn95Asp | |
| ENST00000677028.1:c.266-830A>G | ENSP00000503896.1:n.266-830A>G | |
| ENST00000677029.1:c.-27A>G | ENSP00000502936.1:n.-27A>G | |
| ENST00000677099.1:c.*140A>G | ENSP00000504553.1:n.*140A>G | |
| ENST00000677167.1:c.430A>G | ENSP00000503307.1:p.Asn144Asp | |
| ENST00000677216.1:c.79A>G | ENSP00000503772.1:p.Asn27Asp | |
| ENST00000677293.1:c.-29-1444A>G | ENSP00000504278.1:n.-29-1444A>G | |
| ENST00000677295.1:c.268A>G | ENSP00000504346.1:p.Asn90Asp | |
| ENST00000677586.1:n.181-1347A>G | ||
| ENST00000677626.1:c.268A>G | ENSP00000503552.1:p.Asn90Asp | |
| ENST00000677677.1:n.390A>G | ||
| ENST00000677729.1:c.428-830A>G | ENSP00000503581.1:n.428-830A>G | |
| ENST00000677853.1:c.268A>G | ENSP00000503488.1:p.Asn90Asp | |
| ENST00000678264.1:c.430A>G | ENSP00000503157.1:p.Asn144Asp | |
| ENST00000678303.1:c.340A>G | ENSP00000503696.1:p.Asn114Asp | |
| ENST00000678366.1:c.*613A>G | ENSP00000504353.1:n.*613A>G | |
| ENST00000678546.1:c.268A>G | ENSP00000503062.1:p.Asn90Asp | |
| ENST00000678548.1:c.*140A>G | ENSP00000503934.1:n.*140A>G | |
| ENST00000678626.1:n.122A>G | ||
| ENST00000678707.1:n.178-830A>G | ||
| ENST00000678739.1:c.*488A>G | ENSP00000503806.1:n.*488A>G | |
| ENST00000678785.1:c.268A>G | ENSP00000504231.1:p.Asn90Asp | |
| ENST00000678833.1:c.428-830A>G | ENSP00000503893.1:n.428-830A>G | |
| ENST00000679023.1:c.268A>G | ENSP00000503718.1:p.Asn90Asp | |
| ENST00000679076.1:c.141A>G | ||
| ENST00000679111.1:c.430A>G | ENSP00000504257.1:p.Asn144Asp | |
| ENST00000679189.1:c.79A>G | ENSP00000503356.1:p.Asn27Asp | |
| ENST00000341012.11:c.268A>G | ENSP00000343034.7:p.Asn90Asp | |
| ENST00000372228.7:c.430A>G | ENSP00000361302.3:p.Asn144Asp | |
| ENST00000402686.7:c.430A>G | ENSP00000385797.3:p.Asn144Asp | |
| ENST00000404875.6:c.79A>G | ENSP00000384531.2:p.Asn27Asp | |
| ENST00000415075.5:c.79A>G | ENSP00000405149.1:p.Asn27Asp | |
| ENST00000423007.5:c.430A>G | ENSP00000404119.1:p.Asn144Asp | |
| ENST00000430619.1:c.79A>G | ENSP00000402083.1:p.Asn27Asp | |
| ENST00000441334.5:c.79A>G | ENSP00000395060.1:p.Asn27Asp | |
| ENST00000448212.5:c.268A>G | ENSP00000403736.1:p.Asn90Asp | |
| NM_001077365.1:c.430A>G | NP_001070833.1:p.Asn144Asp | |
| NM_001077366.1:c.268A>G | NP_001070834.1:p.Asn90Asp | |
| NM_001136113.1:c.430A>G | NP_001129585.1:p.Asn144Asp | |
| NM_001136114.1:c.79A>G | NP_001129586.1:p.Asn27Asp | |
| NM_007171.3:c.430A>G | NP_009102.3:p.Asn144Asp | |
| XM_005272156.1:c.430A>G | XP_005272213.1:p.Asn144Asp | |
| XM_005272158.1:c.268A>G | XP_005272215.1:p.Asn90Asp | |
| XM_005272159.1:c.79A>G | XP_005272216.1:p.Asn27Asp | |
| XM_005272162.1:c.-970A>G | XP_005272219.1:n.-970A>G | |
| XM_006716932.1:c.79A>G | XP_006716995.1:p.Asn27Asp | |
| XM_011518140.1:c.283A>G | XP_011516442.1:p.Asn95Asp | |
| XM_011518141.1:c.283A>G | XP_011516443.1:p.Asn95Asp | |
| XM_011518142.1:c.121A>G | XP_011516444.1:p.Asn41Asp | |
| XM_011518143.1:c.176A>G | XP_011516445.1:p.Glu59Gly | |
| XM_011518144.1:c.430A>G | XP_011516446.1:p.Asn144Asp | |
| XM_011518145.1:c.-27A>G | XP_011516447.1:n.-27A>G | |
| XM_011518146.1:c.176A>G | XP_011516448.1:p.Glu59Gly | |
| XR_929703.1:n.606A>G | ||
| NM_001353193.1:c.430A>G | NP_001340122.1:p.Asn144Asp | |
| NM_001353194.1:c.268A>G | NP_001340123.1:p.Asn90Asp | |
| NM_001353195.1:c.79A>G | NP_001340124.1:p.Asn27Asp | |
| NM_001353196.1:c.340A>G | NP_001340125.1:p.Asn114Asp | |
| NM_001353197.1:c.268A>G | NP_001340126.1:p.Asn90Asp | |
| NM_001353198.1:c.268A>G | NP_001340127.1:p.Asn90Asp | |
| NM_001353199.1:c.79A>G | NP_001340128.1:p.Asn27Asp | |
| NM_001353200.1:c.-27A>G | NP_001340129.1:n.-27A>G | |
| NR_148391.1:n.480A>G | ||
| NR_148392.1:n.632A>G | ||
| NR_148393.1:n.480A>G | ||
| NR_148394.1:n.478-830A>G | ||
| NR_148395.1:n.632A>G | ||
| NR_148396.1:n.371-830A>G | ||
| NR_148397.1:n.525A>G | ||
| NR_148398.1:n.480A>G | ||
| NR_148399.1:n.872A>G | ||
| NR_148400.1:n.466A>G | ||
| XM_005272162.3:c.-970A>G | XP_005272219.1:n.-970A>G | |
| XM_006716932.2:c.79A>G | XP_006716995.1:p.Asn27Asp | |
| XM_011518140.2:c.283A>G | XP_011516442.1:p.Asn95Asp | |
| XM_011518141.2:c.283A>G | XP_011516443.1:p.Asn95Asp | |
| XM_011518142.2:c.121A>G | XP_011516444.1:p.Asn41Asp | |
| XM_011518143.2:c.176A>G | XP_011516445.1:p.Glu59Gly | |
| XM_011518145.2:c.-27A>G | XP_011516447.1:n.-27A>G | |
| XM_017014205.2:c.-773A>G | XP_016869694.1:n.-773A>G | |
| XM_024447380.1:c.-707A>G | XP_024303148.1:n.-707A>G | |
| XM_024447381.1:c.-659A>G | XP_024303149.1:n.-659A>G | |
| XM_024447382.1:c.-970A>G | XP_024303150.1:n.-970A>G | |
| XR_001746160.2:n.600A>G | ||
| XR_001746162.2:n.600A>G | ||
| XR_001746164.1:n.378A>G | ||
| XR_001746166.2:n.554A>G | ||
| NM_001077365.2:c.430A>G MANE Select | NP_001070833.1:p.Asn144Asp | |
| NM_001077366.2:c.268A>G | NP_001070834.1:p.Asn90Asp | |
| NM_001136113.2:c.430A>G | NP_001129585.1:p.Asn144Asp | |
| NM_001136114.2:c.79A>G | NP_001129586.1:p.Asn27Asp | |
| NM_001353193.2:c.430A>G | NP_001340122.2:p.Asn144Asp | |
| NM_001353194.2:c.268A>G | NP_001340123.1:p.Asn90Asp | |
| NM_001353195.2:c.79A>G | NP_001340124.1:p.Asn27Asp | |
| NM_001353196.2:c.340A>G | NP_001340125.1:p.Asn114Asp | |
| NM_001353197.2:c.268A>G | NP_001340126.2:p.Asn90Asp | |
| NM_001353198.2:c.268A>G | NP_001340127.2:p.Asn90Asp | |
| NM_001353199.2:c.79A>G | NP_001340128.2:p.Asn27Asp | |
| NM_001353200.2:c.-27A>G | NP_001340129.1:n.-27A>G | |
| NM_001374689.1:c.268A>G | NP_001361618.1:p.Asn90Asp | |
| NM_001374690.1:c.430A>G | NP_001361619.1:p.Asn144Asp | |
| NM_001374691.1:c.79A>G | NP_001361620.1:p.Asn27Asp | |
| NM_001374692.1:c.79A>G | NP_001361621.1:p.Asn27Asp | |
| NM_001374693.1:c.268A>G | NP_001361622.1:p.Asn90Asp | |
| NM_001374695.1:c.-27A>G | NP_001361624.1:n.-27A>G | |
| NM_007171.4:c.430A>G | NP_009102.4:p.Asn144Asp | |
| NR_148391.2:n.464A>G | ||
| NR_148392.2:n.616A>G | ||
| NR_148393.2:n.464A>G | ||
| NR_148394.2:n.462-830A>G | ||
| NR_148395.2:n.616A>G | ||
| NR_148396.2:n.355-830A>G | ||
| NR_148397.2:n.509A>G | ||
| NR_148398.2:n.464A>G | ||
| NR_148399.2:n.856A>G | ||
| NR_148400.2:n.450A>G |