Linked Data
ClinVar Variation Id:
922686
dbSNP Id:
rs1366698322
gnomAD v3:
5-112828929-G-A
gnomAD v4:
5-112828929-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112828929G>A , CM000667.2:g.112828929G>A | GRCh38 |
| NC_000005.9:g.112164626G>A , CM000667.1:g.112164626G>A | GRCh37 |
| NC_000005.8:g.112192525G>A | NCBI36 |
| NG_008481.4:g.141409G>A , LRG_130:g.141409G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000502371.3:c.1409-6022G>A | ENSP00000484935.2:n.1409-6022G>A | |
| ENST00000504915.3:c.1754G>A | ENSP00000473355.2:p.Gly585Glu | |
| ENST00000505084.2:n.1756G>A | ||
| ENST00000505350.2:c.*1706G>A | ENSP00000481752.1:n.*1706G>A | |
| ENST00000507379.6:c.1646G>A | ENSP00000423224.2:p.Gly549Glu | |
| ENST00000509732.6:c.1700G>A | ENSP00000426541.2:p.Gly567Glu | |
| ENST00000512211.7:c.1700G>A | ENSP00000423828.3:p.Gly567Glu | |
| ENST00000257430.9:c.1700G>A MANE Select | ENSP00000257430.4:p.Gly567Glu | |
| ENST00000257430.8:c.1700G>A | ENSP00000257430.4:p.Gly567Glu | |
| ENST00000502371.2:c.97-6022G>A | ||
| ENST00000504915.2:c.389G>A | ENSP00000473355.1:p.Gly130Glu | |
| ENST00000505084.1:n.187G>A | ||
| ENST00000507379.5:c.1646G>A | ENSP00000423224.1:p.Gly549Glu | |
| ENST00000508376.6:c.1700G>A | ENSP00000427089.2:p.Gly567Glu | |
| ENST00000508624.5:c.*1022G>A | ENSP00000424265.1:n.*1022G>A | |
| ENST00000512211.6:c.1700G>A | ENSP00000423828.2:p.Gly567Glu | |
| ENST00000520401.1:c.187G>A | ||
| NM_000038.5:c.1700G>A | NP_000029.2:p.Gly567Glu | |
| NM_001127510.2:c.1700G>A | NP_001120982.1:p.Gly567Glu | |
| NM_001127511.2:c.1646G>A | NP_001120983.2:p.Gly549Glu | |
| NM_001354895.1:c.1700G>A | NP_001341824.1:p.Gly567Glu | |
| NM_001354896.1:c.1754G>A | NP_001341825.1:p.Gly585Glu | |
| NM_001354897.1:c.1730G>A | NP_001341826.1:p.Gly577Glu | |
| NM_001354898.1:c.1625G>A | NP_001341827.1:p.Gly542Glu | |
| NM_001354899.1:c.1616G>A | NP_001341828.1:p.Gly539Glu | |
| NM_001354900.1:c.1577G>A | NP_001341829.1:p.Gly526Glu | |
| NM_001354901.1:c.1523G>A | NP_001341830.1:p.Gly508Glu | |
| NM_001354902.1:c.1427G>A | NP_001341831.1:p.Gly476Glu | |
| NM_001354903.1:c.1397G>A | NP_001341832.1:p.Gly466Glu | |
| NM_001354904.1:c.1322G>A | NP_001341833.1:p.Gly441Glu | |
| NM_001354905.1:c.1220G>A | NP_001341834.1:p.Gly407Glu | |
| NM_001354906.1:c.851G>A | NP_001341835.1:p.Gly284Glu | |
| NM_000038.6:c.1700G>A MANE Select | NP_000029.2:p.Gly567Glu | |
| NM_001127510.3:c.1700G>A | NP_001120982.1:p.Gly567Glu | |
| NM_001127511.3:c.1646G>A | NP_001120983.2:p.Gly549Glu | |
| NM_001354895.2:c.1700G>A | NP_001341824.1:p.Gly567Glu | |
| NM_001354896.2:c.1754G>A | NP_001341825.1:p.Gly585Glu | |
| NM_001354897.2:c.1730G>A | NP_001341826.1:p.Gly577Glu | |
| NM_001354898.2:c.1625G>A | NP_001341827.1:p.Gly542Glu | |
| NM_001354899.2:c.1616G>A | NP_001341828.1:p.Gly539Glu | |
| NM_001354900.2:c.1577G>A | NP_001341829.1:p.Gly526Glu | |
| NM_001354901.2:c.1523G>A | NP_001341830.1:p.Gly508Glu | |
| NM_001354902.2:c.1427G>A | NP_001341831.1:p.Gly476Glu | |
| NM_001354903.2:c.1397G>A | NP_001341832.1:p.Gly466Glu | |
| NM_001354904.2:c.1322G>A | NP_001341833.1:p.Gly441Glu | |
| NM_001354905.2:c.1220G>A | NP_001341834.1:p.Gly407Glu | |
| NM_001354906.2:c.851G>A | NP_001341835.1:p.Gly284Glu |