Linked Data
ClinVar Variation Id:
1761475
ClinVar RCV Id:
RCV002419055
dbSNP Id:
rs2149997379
COSMIC:
COSM1059654
MyVariant Identifiers:
chr5:g.112179274T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112843577T>C , CM000667.2:g.112843577T>C | GRCh38 |
| NC_000005.9:g.112179274T>C , CM000667.1:g.112179274T>C | GRCh37 |
| NC_000005.8:g.112207173T>C | NCBI36 |
| NG_008481.4:g.156057T>C , LRG_130:g.156057T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.8037T>C | ENSP00000473355.2:p.Ile2679= | |
| ENST00000505350.2:c.*7989T>C | ENSP00000481752.1:n.*7989T>C | |
| ENST00000507379.6:c.7929T>C | ENSP00000423224.2:p.Ile2643= | |
| ENST00000509732.6:c.7983T>C | ENSP00000426541.2:p.Ile2661= | |
| ENST00000512211.7:c.7983T>C | ENSP00000423828.3:p.Ile2661= | |
| ENST00000257430.9:c.7983T>C MANE Select | ENSP00000257430.4:p.Ile2661= | |
| ENST00000257430.8:c.7983T>C | ENSP00000257430.4:p.Ile2661= | |
| ENST00000508376.6:c.7983T>C | ENSP00000427089.2:p.Ile2661= | |
| ENST00000520401.1:c.231-13072T>C | ||
| NM_000038.5:c.7983T>C | NP_000029.2:p.Ile2661= | |
| NM_001127510.2:c.7983T>C | NP_001120982.1:p.Ile2661= | |
| NM_001127511.2:c.7929T>C | NP_001120983.2:p.Ile2643= | |
| NM_001354895.1:c.7983T>C | NP_001341824.1:p.Ile2661= | |
| NM_001354896.1:c.8037T>C | NP_001341825.1:p.Ile2679= | |
| NM_001354897.1:c.8013T>C | NP_001341826.1:p.Ile2671= | |
| NM_001354898.1:c.7908T>C | NP_001341827.1:p.Ile2636= | |
| NM_001354899.1:c.7899T>C | NP_001341828.1:p.Ile2633= | |
| NM_001354900.1:c.7860T>C | NP_001341829.1:p.Ile2620= | |
| NM_001354901.1:c.7806T>C | NP_001341830.1:p.Ile2602= | |
| NM_001354902.1:c.7710T>C | NP_001341831.1:p.Ile2570= | |
| NM_001354903.1:c.7680T>C | NP_001341832.1:p.Ile2560= | |
| NM_001354904.1:c.7605T>C | NP_001341833.1:p.Ile2535= | |
| NM_001354905.1:c.7503T>C | NP_001341834.1:p.Ile2501= | |
| NM_001354906.1:c.7134T>C | NP_001341835.1:p.Ile2378= | |
| NM_000038.6:c.7983T>C MANE Select | NP_000029.2:p.Ile2661= | |
| NM_001127510.3:c.7983T>C | NP_001120982.1:p.Ile2661= | |
| NM_001127511.3:c.7929T>C | NP_001120983.2:p.Ile2643= | |
| NM_001354895.2:c.7983T>C | NP_001341824.1:p.Ile2661= | |
| NM_001354896.2:c.8037T>C | NP_001341825.1:p.Ile2679= | |
| NM_001354897.2:c.8013T>C | NP_001341826.1:p.Ile2671= | |
| NM_001354898.2:c.7908T>C | NP_001341827.1:p.Ile2636= | |
| NM_001354899.2:c.7899T>C | NP_001341828.1:p.Ile2633= | |
| NM_001354900.2:c.7860T>C | NP_001341829.1:p.Ile2620= | |
| NM_001354901.2:c.7806T>C | NP_001341830.1:p.Ile2602= | |
| NM_001354902.2:c.7710T>C | NP_001341831.1:p.Ile2570= | |
| NM_001354903.2:c.7680T>C | NP_001341832.1:p.Ile2560= | |
| NM_001354904.2:c.7605T>C | NP_001341833.1:p.Ile2535= | |
| NM_001354905.2:c.7503T>C | NP_001341834.1:p.Ile2501= | |
| NM_001354906.2:c.7134T>C | NP_001341835.1:p.Ile2378= |