Linked Data
ClinVar Variation Id:
482374
dbSNP Id:
rs538571038
ExAC:
5:112176902 G / T
gnomAD v2:
5-112176902-G-T
gnomAD v3:
5-112841205-G-T
gnomAD v4:
5-112841205-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112841205G>T , CM000667.2:g.112841205G>T | GRCh38 |
| NC_000005.9:g.112176902G>T , CM000667.1:g.112176902G>T | GRCh37 |
| NC_000005.8:g.112204801G>T | NCBI36 |
| NG_008481.4:g.153685G>T , LRG_130:g.153685G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.5665G>T | ENSP00000473355.2:p.Asp1889Tyr | |
| ENST00000505350.2:c.*5617G>T | ENSP00000481752.1:n.*5617G>T | |
| ENST00000507379.6:c.5557G>T | ENSP00000423224.2:p.Asp1853Tyr | |
| ENST00000509732.6:c.5611G>T | ENSP00000426541.2:p.Asp1871Tyr | |
| ENST00000512211.7:c.5611G>T | ENSP00000423828.3:p.Asp1871Tyr | |
| ENST00000257430.9:c.5611G>T MANE Select | ENSP00000257430.4:p.Asp1871Tyr | |
| ENST00000257430.8:c.5611G>T | ENSP00000257430.4:p.Asp1871Tyr | |
| ENST00000508376.6:c.5611G>T | ENSP00000427089.2:p.Asp1871Tyr | |
| ENST00000508624.5:c.*4933G>T | ENSP00000424265.1:n.*4933G>T | |
| ENST00000520401.1:c.230+12233G>T | ||
| NM_000038.5:c.5611G>T | NP_000029.2:p.Asp1871Tyr | |
| NM_001127510.2:c.5611G>T | NP_001120982.1:p.Asp1871Tyr | |
| NM_001127511.2:c.5557G>T | NP_001120983.2:p.Asp1853Tyr | |
| NM_001354895.1:c.5611G>T | NP_001341824.1:p.Asp1871Tyr | |
| NM_001354896.1:c.5665G>T | NP_001341825.1:p.Asp1889Tyr | |
| NM_001354897.1:c.5641G>T | NP_001341826.1:p.Asp1881Tyr | |
| NM_001354898.1:c.5536G>T | NP_001341827.1:p.Asp1846Tyr | |
| NM_001354899.1:c.5527G>T | NP_001341828.1:p.Asp1843Tyr | |
| NM_001354900.1:c.5488G>T | NP_001341829.1:p.Asp1830Tyr | |
| NM_001354901.1:c.5434G>T | NP_001341830.1:p.Asp1812Tyr | |
| NM_001354902.1:c.5338G>T | NP_001341831.1:p.Asp1780Tyr | |
| NM_001354903.1:c.5308G>T | NP_001341832.1:p.Asp1770Tyr | |
| NM_001354904.1:c.5233G>T | NP_001341833.1:p.Asp1745Tyr | |
| NM_001354905.1:c.5131G>T | NP_001341834.1:p.Asp1711Tyr | |
| NM_001354906.1:c.4762G>T | NP_001341835.1:p.Asp1588Tyr | |
| NM_000038.6:c.5611G>T MANE Select | NP_000029.2:p.Asp1871Tyr | |
| NM_001127510.3:c.5611G>T | NP_001120982.1:p.Asp1871Tyr | |
| NM_001127511.3:c.5557G>T | NP_001120983.2:p.Asp1853Tyr | |
| NM_001354895.2:c.5611G>T | NP_001341824.1:p.Asp1871Tyr | |
| NM_001354896.2:c.5665G>T | NP_001341825.1:p.Asp1889Tyr | |
| NM_001354897.2:c.5641G>T | NP_001341826.1:p.Asp1881Tyr | |
| NM_001354898.2:c.5536G>T | NP_001341827.1:p.Asp1846Tyr | |
| NM_001354899.2:c.5527G>T | NP_001341828.1:p.Asp1843Tyr | |
| NM_001354900.2:c.5488G>T | NP_001341829.1:p.Asp1830Tyr | |
| NM_001354901.2:c.5434G>T | NP_001341830.1:p.Asp1812Tyr | |
| NM_001354902.2:c.5338G>T | NP_001341831.1:p.Asp1780Tyr | |
| NM_001354903.2:c.5308G>T | NP_001341832.1:p.Asp1770Tyr | |
| NM_001354904.2:c.5233G>T | NP_001341833.1:p.Asp1745Tyr | |
| NM_001354905.2:c.5131G>T | NP_001341834.1:p.Asp1711Tyr | |
| NM_001354906.2:c.4762G>T | NP_001341835.1:p.Asp1588Tyr |