Linked Data
ClinVar Variation Id:
166896
dbSNP Id:
rs142057517
ExAC:
9:134390889 G / A
gnomAD v2:
9-134390889-G-A
gnomAD v3:
9-131515502-G-A
gnomAD v4:
9-131515502-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.131515502G>A , CM000671.2:g.131515502G>A | GRCh38 |
| NC_000009.11:g.134390889G>A , CM000671.1:g.134390889G>A | GRCh37 |
| NC_000009.10:g.133380710G>A | NCBI36 |
| NG_008896.1:g.17601G>A | |
| NG_008896.2:g.17601G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000341012.13:c.1090G>A | ENSP00000343034.7:p.Ala364Thr | |
| ENST00000404875.7:n.1792G>A | ||
| ENST00000423007.6:c.1309G>A | ENSP00000404119.2:p.Ala437Thr | |
| ENST00000677295.2:c.*1596G>A | ENSP00000504346.2:n.*1596G>A | |
| ENST00000678264.2:c.*1435G>A | ENSP00000503157.2:n.*1435G>A | |
| ENST00000682070.1:n.1717G>A | ||
| ENST00000682539.1:c.77G>A | ||
| ENST00000682813.1:n.1517G>A | ||
| ENST00000683392.1:n.3999G>A | ||
| ENST00000683712.1:n.1657G>A | ||
| ENST00000683900.1:n.3152G>A | ||
| ENST00000684062.1:n.1918G>A | ||
| ENST00000684579.1:n.3098G>A | ||
| ENST00000341012.12:c.1090G>A | ENSP00000343034.7:p.Ala364Thr | |
| ENST00000372220.5:c.121G>A | ENSP00000361294.5:p.Ala41Thr | |
| ENST00000372228.9:c.1318G>A | ENSP00000361302.3:p.Ala440Thr | |
| ENST00000402686.8:c.1252G>A MANE Select | ENSP00000385797.4:p.Ala418Thr | |
| ENST00000676640.1:c.1252G>A | ENSP00000503281.1:p.Ala418Thr | |
| ENST00000676803.1:c.427G>A | ENSP00000503093.1:p.Ala143Thr | |
| ENST00000676835.1:c.*467G>A | ENSP00000502911.1:n.*467G>A | |
| ENST00000677029.1:c.796G>A | ENSP00000502936.1:p.Ala266Thr | |
| ENST00000677099.1:c.*962G>A | ENSP00000504553.1:n.*962G>A | |
| ENST00000677216.1:c.901G>A | ENSP00000503772.1:p.Ala301Thr | |
| ENST00000677295.1:c.*629G>A | ENSP00000504346.1:n.*629G>A | |
| ENST00000677444.1:c.1058G>A | ||
| ENST00000677586.1:n.733G>A | ||
| ENST00000677626.1:c.901G>A | ENSP00000503552.1:p.Ala301Thr | |
| ENST00000677677.1:n.1212G>A | ||
| ENST00000677853.1:c.*260G>A | ENSP00000503488.1:n.*260G>A | |
| ENST00000677944.1:c.514G>A | ||
| ENST00000678264.1:c.*629G>A | ENSP00000503157.1:n.*629G>A | |
| ENST00000678303.1:c.1162G>A | ENSP00000503696.1:p.Ala388Thr | |
| ENST00000678366.1:c.*1501G>A | ENSP00000504353.1:n.*1501G>A | |
| ENST00000678546.1:c.*1197G>A | ENSP00000503062.1:n.*1197G>A | |
| ENST00000678548.1:c.*1324G>A | ENSP00000503934.1:n.*1324G>A | |
| ENST00000678626.1:n.949G>A | ||
| ENST00000678733.1:c.333G>A | ||
| ENST00000678739.1:c.*1578G>A | ENSP00000503806.1:n.*1578G>A | |
| ENST00000678795.1:n.339G>A | ||
| ENST00000678833.1:c.*699G>A | ENSP00000503893.1:n.*699G>A | |
| ENST00000678942.1:c.432G>A | ENSP00000504690.1:n.432G>A | |
| ENST00000679023.1:c.1090G>A | ENSP00000503718.1:p.Ala364Thr | |
| ENST00000679076.1:c.871G>A | ||
| ENST00000679111.1:c.1252G>A | ENSP00000504257.1:p.Ala418Thr | |
| ENST00000679189.1:c.901G>A | ENSP00000503356.1:p.Ala301Thr | |
| ENST00000341012.11:c.1090G>A | ENSP00000343034.7:p.Ala364Thr | |
| ENST00000372228.7:c.1318G>A | ENSP00000361302.3:p.Ala440Thr | |
| ENST00000402686.7:c.1252G>A | ENSP00000385797.3:p.Ala418Thr | |
| ENST00000404875.6:c.901G>A | ENSP00000384531.2:p.Ala301Thr | |
| ENST00000423007.5:c.1252G>A | ENSP00000404119.1:p.Ala418Thr | |
| ENST00000485278.5:n.1807G>A | ||
| NM_001077365.1:c.1252G>A | NP_001070833.1:p.Ala418Thr | |
| NM_001077366.1:c.1090G>A | NP_001070834.1:p.Ala364Thr | |
| NM_001136113.1:c.1252G>A | NP_001129585.1:p.Ala418Thr | |
| NM_001136114.1:c.901G>A | NP_001129586.1:p.Ala301Thr | |
| NM_007171.3:c.1318G>A | NP_009102.3:p.Ala440Thr | |
| XM_005272156.1:c.1318G>A | XP_005272213.1:p.Ala440Thr | |
| XM_005272158.1:c.1156G>A | XP_005272215.1:p.Ala386Thr | |
| XM_005272159.1:c.967G>A | XP_005272216.1:p.Ala323Thr | |
| XM_005272162.1:c.121G>A | XP_005272219.1:p.Ala41Thr | |
| XM_006716932.1:c.967G>A | XP_006716995.1:p.Ala323Thr | |
| XM_011518140.1:c.1171G>A | XP_011516442.1:p.Ala391Thr | |
| XM_011518141.1:c.1105G>A | XP_011516443.1:p.Ala369Thr | |
| XM_011518142.1:c.1009G>A | XP_011516444.1:p.Ala337Thr | |
| XM_011518143.1:c.1003G>A | XP_011516445.1:p.Ala335Thr | |
| XM_011518144.1:c.1318G>A | XP_011516446.1:p.Ala440Thr | |
| XM_011518145.1:c.862G>A | XP_011516447.1:p.Ala288Thr | |
| XM_011518146.1:c.1003G>A | XP_011516448.1:p.Ala335Thr | |
| XR_929703.1:n.1494G>A | ||
| NM_001353193.1:c.1318G>A | NP_001340122.1:p.Ala440Thr | |
| NM_001353194.1:c.1090G>A | NP_001340123.1:p.Ala364Thr | |
| NM_001353195.1:c.901G>A | NP_001340124.1:p.Ala301Thr | |
| NM_001353196.1:c.1162G>A | NP_001340125.1:p.Ala388Thr | |
| NM_001353197.1:c.1156G>A | NP_001340126.1:p.Ala386Thr | |
| NM_001353198.1:c.1156G>A | NP_001340127.1:p.Ala386Thr | |
| NM_001353199.1:c.967G>A | NP_001340128.1:p.Ala323Thr | |
| NM_001353200.1:c.796G>A | NP_001340129.1:p.Ala266Thr | |
| NR_148391.1:n.1302G>A | ||
| NR_148392.1:n.1520G>A | ||
| NR_148393.1:n.1302G>A | ||
| NR_148394.1:n.1195G>A | ||
| NR_148395.1:n.1454G>A | ||
| NR_148396.1:n.1088G>A | ||
| NR_148397.1:n.1352G>A | ||
| NR_148398.1:n.1307G>A | ||
| NR_148399.1:n.1694G>A | ||
| NR_148400.1:n.1293G>A | ||
| XM_005272162.3:c.121G>A | XP_005272219.1:p.Ala41Thr | |
| XM_006716932.2:c.967G>A | XP_006716995.1:p.Ala323Thr | |
| XM_011518140.2:c.1171G>A | XP_011516442.1:p.Ala391Thr | |
| XM_011518141.2:c.1105G>A | XP_011516443.1:p.Ala369Thr | |
| XM_011518142.2:c.1009G>A | XP_011516444.1:p.Ala337Thr | |
| XM_011518143.2:c.1003G>A | XP_011516445.1:p.Ala335Thr | |
| XM_011518145.2:c.862G>A | XP_011516447.1:p.Ala288Thr | |
| XM_017014205.2:c.121G>A | XP_016869694.1:p.Ala41Thr | |
| XM_024447380.1:c.121G>A | XP_024303148.1:p.Ala41Thr | |
| XM_024447381.1:c.427G>A | XP_024303149.1:p.Ala143Thr | |
| XM_024447382.1:c.121G>A | XP_024303150.1:p.Ala41Thr | |
| XR_001746160.2:n.1422G>A | ||
| XR_001746162.2:n.1488G>A | ||
| XR_001746164.1:n.1205G>A | ||
| XR_001746166.2:n.1639G>A | ||
| NM_001077365.2:c.1252G>A MANE Select | NP_001070833.1:p.Ala418Thr | |
| NM_001077366.2:c.1090G>A | NP_001070834.1:p.Ala364Thr | |
| NM_001136113.2:c.1252G>A | NP_001129585.1:p.Ala418Thr | |
| NM_001136114.2:c.901G>A | NP_001129586.1:p.Ala301Thr | |
| NM_001353193.2:c.1318G>A | NP_001340122.2:p.Ala440Thr | |
| NM_001353194.2:c.1090G>A | NP_001340123.1:p.Ala364Thr | |
| NM_001353195.2:c.901G>A | NP_001340124.1:p.Ala301Thr | |
| NM_001353196.2:c.1162G>A | NP_001340125.1:p.Ala388Thr | |
| NM_001353197.2:c.1156G>A | NP_001340126.2:p.Ala386Thr | |
| NM_001353198.2:c.1156G>A | NP_001340127.2:p.Ala386Thr | |
| NM_001353199.2:c.967G>A | NP_001340128.2:p.Ala323Thr | |
| NM_001353200.2:c.796G>A | NP_001340129.1:p.Ala266Thr | |
| NM_001374689.1:c.1240G>A | NP_001361618.1:p.Ala414Thr | |
| NM_001374690.1:c.1252G>A | NP_001361619.1:p.Ala418Thr | |
| NM_001374691.1:c.901G>A | NP_001361620.1:p.Ala301Thr | |
| NM_001374692.1:c.901G>A | NP_001361621.1:p.Ala301Thr | |
| NM_001374693.1:c.901G>A | NP_001361622.1:p.Ala301Thr | |
| NM_001374695.1:c.862G>A | NP_001361624.1:p.Ala288Thr | |
| NM_007171.4:c.1318G>A | NP_009102.4:p.Ala440Thr | |
| NR_148391.2:n.1286G>A | ||
| NR_148392.2:n.1504G>A | ||
| NR_148393.2:n.1286G>A | ||
| NR_148394.2:n.1179G>A | ||
| NR_148395.2:n.1438G>A | ||
| NR_148396.2:n.1072G>A | ||
| NR_148397.2:n.1336G>A | ||
| NR_148398.2:n.1291G>A | ||
| NR_148399.2:n.1678G>A | ||
| NR_148400.2:n.1277G>A |