Linked Data
ClinVar Variation Id:
188287
dbSNP Id:
rs199700509
ExAC:
7:6026568 T / C
gnomAD v2:
7-6026568-T-C
gnomAD v3:
7-5986937-T-C
gnomAD v4:
7-5986937-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.5986937T>C , CM000669.2:g.5986937T>C | GRCh38 |
| NC_000007.13:g.6026568T>C , CM000669.1:g.6026568T>C | GRCh37 |
| NC_000007.12:g.5993094T>C | NCBI36 |
| NG_008466.1:g.27170A>G , LRG_161:g.27170A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000699814.2:c.*1224A>G | ENSP00000514615.2:n.*1224A>G | |
| ENST00000699840.2:c.1825A>G | ENSP00000514638.2:p.Lys609Glu | |
| ENST00000699930.2:c.1720A>G | ENSP00000514695.2:p.Lys574Glu | |
| ENST00000406569.8:c.1678+150A>G | ENSP00000514464.1:n.1678+150A>G | |
| ENST00000644110.2:c.*1422A>G | ENSP00000496392.2:n.*1422A>G | |
| ENST00000699752.1:c.1672A>G | ENSP00000514561.1:p.Lys558Glu | |
| ENST00000699753.1:c.*1249A>G | ENSP00000514562.1:n.*1249A>G | |
| ENST00000699754.1:c.1630A>G | ENSP00000514563.1:p.Lys544Glu | |
| ENST00000699755.1:c.*1227A>G | ENSP00000514564.1:n.*1227A>G | |
| ENST00000699756.1:c.*1415A>G | ENSP00000514565.1:n.*1415A>G | |
| ENST00000699757.1:c.*1085A>G | ENSP00000514566.1:n.*1085A>G | |
| ENST00000699758.1:c.*1085A>G | ENSP00000514567.1:n.*1085A>G | |
| ENST00000699759.1:n.2682A>G | ||
| ENST00000699760.1:c.1510A>G | ENSP00000514568.1:p.Lys504Glu | |
| ENST00000699761.1:c.1423A>G | ENSP00000514569.1:p.Lys475Glu | |
| ENST00000699762.1:c.1255A>G | ENSP00000514570.1:p.Lys419Glu | |
| ENST00000699763.1:c.*918A>G | ENSP00000514571.1:n.*918A>G | |
| ENST00000699764.1:c.*146A>G | ENSP00000514572.1:n.*146A>G | |
| ENST00000699765.1:c.*924A>G | ENSP00000514573.1:n.*924A>G | |
| ENST00000699766.1:c.1828A>G | ENSP00000514574.1:p.Lys610Glu | |
| ENST00000699767.1:c.1828A>G | ENSP00000514575.1:p.Lys610Glu | |
| ENST00000699768.1:c.1828A>G | ENSP00000514576.1:p.Lys610Glu | |
| ENST00000699811.1:c.1423A>G | ENSP00000514614.1:p.Lys475Glu | |
| ENST00000699813.1:n.1941A>G | ||
| ENST00000699814.1:c.1451A>G | ||
| ENST00000699815.1:c.*1359A>G | ENSP00000514616.1:n.*1359A>G | |
| ENST00000699816.1:c.*718A>G | ENSP00000514617.1:n.*718A>G | |
| ENST00000699817.1:c.*1422A>G | ENSP00000514618.1:n.*1422A>G | |
| ENST00000699818.1:c.1423A>G | ENSP00000514619.1:p.Lys475Glu | |
| ENST00000699819.1:c.*985A>G | ENSP00000514620.1:n.*985A>G | |
| ENST00000699820.1:c.1144+2863A>G | ENSP00000514621.1:n.1144+2863A>G | |
| ENST00000699821.1:c.1423A>G | ENSP00000514622.1:p.Lys475Glu | |
| ENST00000699822.1:c.*1280A>G | ENSP00000514623.1:n.*1280A>G | |
| ENST00000699823.1:c.1423A>G | ENSP00000514624.1:p.Lys475Glu | |
| ENST00000699824.1:c.*1331A>G | ENSP00000514625.1:n.*1331A>G | |
| ENST00000699825.1:c.1267A>G | ENSP00000514626.1:p.Lys423Glu | |
| ENST00000699826.1:c.*1227A>G | ENSP00000514627.1:n.*1227A>G | |
| ENST00000699827.1:c.1660A>G | ENSP00000514628.1:p.Lys554Glu | |
| ENST00000699828.1:c.*918A>G | ENSP00000514629.1:n.*918A>G | |
| ENST00000699833.1:n.3600A>G | ||
| ENST00000699837.1:c.1423A>G | ENSP00000514635.1:p.Lys475Glu | |
| ENST00000699838.1:c.*1728A>G | ENSP00000514636.1:n.*1728A>G | |
| ENST00000699839.1:c.2014A>G | ENSP00000514637.1:p.Lys672Glu | |
| ENST00000699916.1:c.*1085A>G | ENSP00000514684.1:n.*1085A>G | |
| ENST00000699917.1:c.*1277A>G | ENSP00000514685.1:n.*1277A>G | |
| ENST00000699918.1:c.*1329A>G | ENSP00000514686.1:n.*1329A>G | |
| ENST00000699919.1:c.*1415A>G | ENSP00000514687.1:n.*1415A>G | |
| ENST00000699920.1:c.*1464A>G | ENSP00000514688.1:n.*1464A>G | |
| ENST00000699928.1:c.989-3946A>G | ENSP00000514693.1:n.989-3946A>G | |
| ENST00000699951.1:c.*924A>G | ENSP00000514706.1:n.*924A>G | |
| ENST00000699952.1:c.803+10389A>G | ENSP00000514707.1:n.803+10389A>G | |
| ENST00000265849.12:c.1828A>G MANE Select | ENSP00000265849.7:p.Lys610Glu | |
| ENST00000642292.1:c.1423A>G | ENSP00000495524.1:p.Lys475Glu | |
| ENST00000642456.1:c.1423A>G | ENSP00000493814.1:p.Lys475Glu | |
| ENST00000643595.1:c.*1227A>G | ENSP00000494497.1:n.*1227A>G | |
| ENST00000644110.1:c.1510A>G | ENSP00000496392.1:p.Lys504Glu | |
| ENST00000265849.11:c.1828A>G | ENSP00000265849.7:p.Lys610Glu | |
| ENST00000382321.5:c.804-3946A>G | ENSP00000371758.4:n.804-3946A>G | |
| ENST00000406569.7:n.1678+150A>G | ||
| ENST00000441476.6:c.1510A>G | ENSP00000392843.2:p.Lys504Glu | |
| ENST00000469652.1:n.63-4032A>G | ||
| NM_000535.5:c.1828A>G , LRG_161t1:c.1828A>G | NP_000526.1:p.Lys610Glu | |
| NR_003085.2:n.1910A>G | ||
| XM_006715742.2:c.1822A>G | XP_006715805.1:p.Lys608Glu | |
| XM_006715744.2:c.895A>G | XP_006715807.1:p.Lys299Glu | |
| XM_011515427.1:c.1873A>G | XP_011513729.1:p.Lys625Glu | |
| XM_011515428.1:c.1717A>G | XP_011513730.1:p.Lys573Glu | |
| XM_011515429.1:c.1510A>G | XP_011513731.1:p.Lys504Glu | |
| XM_011515430.1:c.1510A>G | XP_011513732.1:p.Lys504Glu | |
| NM_000535.6:c.1828A>G | NP_000526.2:p.Lys610Glu | |
| NM_001322003.1:c.1423A>G | NP_001308932.1:p.Lys475Glu | |
| NM_001322004.1:c.1423A>G | NP_001308933.1:p.Lys475Glu | |
| NM_001322005.1:c.1423A>G | NP_001308934.1:p.Lys475Glu | |
| NM_001322006.1:c.1672A>G | NP_001308935.1:p.Lys558Glu | |
| NM_001322007.1:c.1510A>G | NP_001308936.1:p.Lys504Glu | |
| NM_001322008.1:c.1510A>G | NP_001308937.1:p.Lys504Glu | |
| NM_001322009.1:c.1423A>G | NP_001308938.1:p.Lys475Glu | |
| NM_001322010.1:c.1267A>G | NP_001308939.1:p.Lys423Glu | |
| NM_001322011.1:c.895A>G | NP_001308940.1:p.Lys299Glu | |
| NM_001322012.1:c.895A>G | NP_001308941.1:p.Lys299Glu | |
| NM_001322013.1:c.1255A>G | NP_001308942.1:p.Lys419Glu | |
| NM_001322014.1:c.1828A>G | NP_001308943.1:p.Lys610Glu | |
| NM_001322015.1:c.1519A>G | NP_001308944.1:p.Lys507Glu | |
| NR_136154.1:n.1915A>G | ||
| XM_006715744.4:c.895A>G | XP_006715807.1:p.Lys299Glu | |
| XM_017012342.2:c.895A>G | XP_016867831.1:p.Lys299Glu | |
| XM_024446800.1:c.1267A>G | XP_024302568.1:p.Lys423Glu | |
| NM_000535.7:c.1828A>G MANE Select | NP_000526.2:p.Lys610Glu | |
| NM_001322003.2:c.1423A>G | NP_001308932.1:p.Lys475Glu | |
| NM_001322004.2:c.1423A>G | NP_001308933.1:p.Lys475Glu | |
| NM_001322005.2:c.1423A>G | NP_001308934.1:p.Lys475Glu | |
| NM_001322006.2:c.1672A>G | NP_001308935.1:p.Lys558Glu | |
| NM_001322008.2:c.1510A>G | NP_001308937.1:p.Lys504Glu | |
| NM_001322009.2:c.1423A>G | NP_001308938.1:p.Lys475Glu | |
| NM_001322010.2:c.1267A>G | NP_001308939.1:p.Lys423Glu | |
| NM_001322011.2:c.895A>G | NP_001308940.1:p.Lys299Glu | |
| NM_001322012.2:c.895A>G | NP_001308941.1:p.Lys299Glu | |
| NM_001322013.2:c.1255A>G | NP_001308942.1:p.Lys419Glu | |
| NM_001322014.2:c.1828A>G | NP_001308943.1:p.Lys610Glu | |
| NM_001322015.2:c.1519A>G | NP_001308944.1:p.Lys507Glu | |
| NM_001322007.2:c.1510A>G | NP_001308936.1:p.Lys504Glu |