Linked Data
ClinVar Variation Id:
233218
dbSNP Id:
rs769889352
ExAC:
5:112178769 T / C
gnomAD v2:
5-112178769-T-C
gnomAD v3:
5-112843072-T-C
gnomAD v4:
5-112843072-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112843072T>C , CM000667.2:g.112843072T>C | GRCh38 |
| NC_000005.9:g.112178769T>C , CM000667.1:g.112178769T>C | GRCh37 |
| NC_000005.8:g.112206668T>C | NCBI36 |
| NG_008481.4:g.155552T>C , LRG_130:g.155552T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.7532T>C | ENSP00000473355.2:p.Leu2511Pro | |
| ENST00000505350.2:c.*7484T>C | ENSP00000481752.1:n.*7484T>C | |
| ENST00000507379.6:c.7424T>C | ENSP00000423224.2:p.Leu2475Pro | |
| ENST00000509732.6:c.7478T>C | ENSP00000426541.2:p.Leu2493Pro | |
| ENST00000512211.7:c.7478T>C | ENSP00000423828.3:p.Leu2493Pro | |
| ENST00000257430.9:c.7478T>C MANE Select | ENSP00000257430.4:p.Leu2493Pro | |
| ENST00000257430.8:c.7478T>C | ENSP00000257430.4:p.Leu2493Pro | |
| ENST00000508376.6:c.7478T>C | ENSP00000427089.2:p.Leu2493Pro | |
| ENST00000520401.1:c.231-13577T>C | ||
| NM_000038.5:c.7478T>C | NP_000029.2:p.Leu2493Pro | |
| NM_001127510.2:c.7478T>C | NP_001120982.1:p.Leu2493Pro | |
| NM_001127511.2:c.7424T>C | NP_001120983.2:p.Leu2475Pro | |
| NM_001354895.1:c.7478T>C | NP_001341824.1:p.Leu2493Pro | |
| NM_001354896.1:c.7532T>C | NP_001341825.1:p.Leu2511Pro | |
| NM_001354897.1:c.7508T>C | NP_001341826.1:p.Leu2503Pro | |
| NM_001354898.1:c.7403T>C | NP_001341827.1:p.Leu2468Pro | |
| NM_001354899.1:c.7394T>C | NP_001341828.1:p.Leu2465Pro | |
| NM_001354900.1:c.7355T>C | NP_001341829.1:p.Leu2452Pro | |
| NM_001354901.1:c.7301T>C | NP_001341830.1:p.Leu2434Pro | |
| NM_001354902.1:c.7205T>C | NP_001341831.1:p.Leu2402Pro | |
| NM_001354903.1:c.7175T>C | NP_001341832.1:p.Leu2392Pro | |
| NM_001354904.1:c.7100T>C | NP_001341833.1:p.Leu2367Pro | |
| NM_001354905.1:c.6998T>C | NP_001341834.1:p.Leu2333Pro | |
| NM_001354906.1:c.6629T>C | NP_001341835.1:p.Leu2210Pro | |
| NM_000038.6:c.7478T>C MANE Select | NP_000029.2:p.Leu2493Pro | |
| NM_001127510.3:c.7478T>C | NP_001120982.1:p.Leu2493Pro | |
| NM_001127511.3:c.7424T>C | NP_001120983.2:p.Leu2475Pro | |
| NM_001354895.2:c.7478T>C | NP_001341824.1:p.Leu2493Pro | |
| NM_001354896.2:c.7532T>C | NP_001341825.1:p.Leu2511Pro | |
| NM_001354897.2:c.7508T>C | NP_001341826.1:p.Leu2503Pro | |
| NM_001354898.2:c.7403T>C | NP_001341827.1:p.Leu2468Pro | |
| NM_001354899.2:c.7394T>C | NP_001341828.1:p.Leu2465Pro | |
| NM_001354900.2:c.7355T>C | NP_001341829.1:p.Leu2452Pro | |
| NM_001354901.2:c.7301T>C | NP_001341830.1:p.Leu2434Pro | |
| NM_001354902.2:c.7205T>C | NP_001341831.1:p.Leu2402Pro | |
| NM_001354903.2:c.7175T>C | NP_001341832.1:p.Leu2392Pro | |
| NM_001354904.2:c.7100T>C | NP_001341833.1:p.Leu2367Pro | |
| NM_001354905.2:c.6998T>C | NP_001341834.1:p.Leu2333Pro | |
| NM_001354906.2:c.6629T>C | NP_001341835.1:p.Leu2210Pro |