Linked Data
ClinVar Variation Id:
1474360
ClinVar RCV Id:
RCV003773096
dbSNP Id:
rs2149932434
COSMIC:
COSM5025155
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112840711C>T , CM000667.2:g.112840711C>T | GRCh38 |
| NC_000005.9:g.112176408C>T , CM000667.1:g.112176408C>T | GRCh37 |
| NC_000005.8:g.112204307C>T | NCBI36 |
| NG_008481.4:g.153191C>T , LRG_130:g.153191C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.5171C>T | ENSP00000473355.2:p.Ser1724Leu | |
| ENST00000505350.2:c.*5123C>T | ENSP00000481752.1:n.*5123C>T | |
| ENST00000507379.6:c.5063C>T | ENSP00000423224.2:p.Ser1688Leu | |
| ENST00000509732.6:c.5117C>T | ENSP00000426541.2:p.Ser1706Leu | |
| ENST00000512211.7:c.5117C>T | ENSP00000423828.3:p.Ser1706Leu | |
| ENST00000257430.9:c.5117C>T MANE Select | ENSP00000257430.4:p.Ser1706Leu | |
| ENST00000257430.8:c.5117C>T | ENSP00000257430.4:p.Ser1706Leu | |
| ENST00000508376.6:c.5117C>T | ENSP00000427089.2:p.Ser1706Leu | |
| ENST00000508624.5:c.*4439C>T | ENSP00000424265.1:n.*4439C>T | |
| ENST00000520401.1:c.230+11739C>T | ||
| NM_000038.5:c.5117C>T | NP_000029.2:p.Ser1706Leu | |
| NM_001127510.2:c.5117C>T | NP_001120982.1:p.Ser1706Leu | |
| NM_001127511.2:c.5063C>T | NP_001120983.2:p.Ser1688Leu | |
| NM_001354895.1:c.5117C>T | NP_001341824.1:p.Ser1706Leu | |
| NM_001354896.1:c.5171C>T | NP_001341825.1:p.Ser1724Leu | |
| NM_001354897.1:c.5147C>T | NP_001341826.1:p.Ser1716Leu | |
| NM_001354898.1:c.5042C>T | NP_001341827.1:p.Ser1681Leu | |
| NM_001354899.1:c.5033C>T | NP_001341828.1:p.Ser1678Leu | |
| NM_001354900.1:c.4994C>T | NP_001341829.1:p.Ser1665Leu | |
| NM_001354901.1:c.4940C>T | NP_001341830.1:p.Ser1647Leu | |
| NM_001354902.1:c.4844C>T | NP_001341831.1:p.Ser1615Leu | |
| NM_001354903.1:c.4814C>T | NP_001341832.1:p.Ser1605Leu | |
| NM_001354904.1:c.4739C>T | NP_001341833.1:p.Ser1580Leu | |
| NM_001354905.1:c.4637C>T | NP_001341834.1:p.Ser1546Leu | |
| NM_001354906.1:c.4268C>T | NP_001341835.1:p.Ser1423Leu | |
| NM_000038.6:c.5117C>T MANE Select | NP_000029.2:p.Ser1706Leu | |
| NM_001127510.3:c.5117C>T | NP_001120982.1:p.Ser1706Leu | |
| NM_001127511.3:c.5063C>T | NP_001120983.2:p.Ser1688Leu | |
| NM_001354895.2:c.5117C>T | NP_001341824.1:p.Ser1706Leu | |
| NM_001354896.2:c.5171C>T | NP_001341825.1:p.Ser1724Leu | |
| NM_001354897.2:c.5147C>T | NP_001341826.1:p.Ser1716Leu | |
| NM_001354898.2:c.5042C>T | NP_001341827.1:p.Ser1681Leu | |
| NM_001354899.2:c.5033C>T | NP_001341828.1:p.Ser1678Leu | |
| NM_001354900.2:c.4994C>T | NP_001341829.1:p.Ser1665Leu | |
| NM_001354901.2:c.4940C>T | NP_001341830.1:p.Ser1647Leu | |
| NM_001354902.2:c.4844C>T | NP_001341831.1:p.Ser1615Leu | |
| NM_001354903.2:c.4814C>T | NP_001341832.1:p.Ser1605Leu | |
| NM_001354904.2:c.4739C>T | NP_001341833.1:p.Ser1580Leu | |
| NM_001354905.2:c.4637C>T | NP_001341834.1:p.Ser1546Leu | |
| NM_001354906.2:c.4268C>T | NP_001341835.1:p.Ser1423Leu |