Linked Data
ClinVar Variation Id:
411520
dbSNP Id:
rs1060503346
gnomAD v2:
5-112176363-C-T
gnomAD v3:
5-112840666-C-T
gnomAD v4:
5-112840666-C-T
COSMIC:
COSM4992204
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112840666C>T , CM000667.2:g.112840666C>T | GRCh38 |
| NC_000005.9:g.112176363C>T , CM000667.1:g.112176363C>T | GRCh37 |
| NC_000005.8:g.112204262C>T | NCBI36 |
| NG_008481.4:g.153146C>T , LRG_130:g.153146C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.5126C>T | ENSP00000473355.2:p.Pro1709Leu | |
| ENST00000505350.2:c.*5078C>T | ENSP00000481752.1:n.*5078C>T | |
| ENST00000507379.6:c.5018C>T | ENSP00000423224.2:p.Pro1673Leu | |
| ENST00000509732.6:c.5072C>T | ENSP00000426541.2:p.Pro1691Leu | |
| ENST00000512211.7:c.5072C>T | ENSP00000423828.3:p.Pro1691Leu | |
| ENST00000257430.9:c.5072C>T MANE Select | ENSP00000257430.4:p.Pro1691Leu | |
| ENST00000257430.8:c.5072C>T | ENSP00000257430.4:p.Pro1691Leu | |
| ENST00000508376.6:c.5072C>T | ENSP00000427089.2:p.Pro1691Leu | |
| ENST00000508624.5:c.*4394C>T | ENSP00000424265.1:n.*4394C>T | |
| ENST00000520401.1:c.230+11694C>T | ||
| NM_000038.5:c.5072C>T | NP_000029.2:p.Pro1691Leu | |
| NM_001127510.2:c.5072C>T | NP_001120982.1:p.Pro1691Leu | |
| NM_001127511.2:c.5018C>T | NP_001120983.2:p.Pro1673Leu | |
| NM_001354895.1:c.5072C>T | NP_001341824.1:p.Pro1691Leu | |
| NM_001354896.1:c.5126C>T | NP_001341825.1:p.Pro1709Leu | |
| NM_001354897.1:c.5102C>T | NP_001341826.1:p.Pro1701Leu | |
| NM_001354898.1:c.4997C>T | NP_001341827.1:p.Pro1666Leu | |
| NM_001354899.1:c.4988C>T | NP_001341828.1:p.Pro1663Leu | |
| NM_001354900.1:c.4949C>T | NP_001341829.1:p.Pro1650Leu | |
| NM_001354901.1:c.4895C>T | NP_001341830.1:p.Pro1632Leu | |
| NM_001354902.1:c.4799C>T | NP_001341831.1:p.Pro1600Leu | |
| NM_001354903.1:c.4769C>T | NP_001341832.1:p.Pro1590Leu | |
| NM_001354904.1:c.4694C>T | NP_001341833.1:p.Pro1565Leu | |
| NM_001354905.1:c.4592C>T | NP_001341834.1:p.Pro1531Leu | |
| NM_001354906.1:c.4223C>T | NP_001341835.1:p.Pro1408Leu | |
| NM_000038.6:c.5072C>T MANE Select | NP_000029.2:p.Pro1691Leu | |
| NM_001127510.3:c.5072C>T | NP_001120982.1:p.Pro1691Leu | |
| NM_001127511.3:c.5018C>T | NP_001120983.2:p.Pro1673Leu | |
| NM_001354895.2:c.5072C>T | NP_001341824.1:p.Pro1691Leu | |
| NM_001354896.2:c.5126C>T | NP_001341825.1:p.Pro1709Leu | |
| NM_001354897.2:c.5102C>T | NP_001341826.1:p.Pro1701Leu | |
| NM_001354898.2:c.4997C>T | NP_001341827.1:p.Pro1666Leu | |
| NM_001354899.2:c.4988C>T | NP_001341828.1:p.Pro1663Leu | |
| NM_001354900.2:c.4949C>T | NP_001341829.1:p.Pro1650Leu | |
| NM_001354901.2:c.4895C>T | NP_001341830.1:p.Pro1632Leu | |
| NM_001354902.2:c.4799C>T | NP_001341831.1:p.Pro1600Leu | |
| NM_001354903.2:c.4769C>T | NP_001341832.1:p.Pro1590Leu | |
| NM_001354904.2:c.4694C>T | NP_001341833.1:p.Pro1565Leu | |
| NM_001354905.2:c.4592C>T | NP_001341834.1:p.Pro1531Leu | |
| NM_001354906.2:c.4223C>T | NP_001341835.1:p.Pro1408Leu |