Linked Data
dbSNP Id:
rs143342566
ExAC:
3:184045037 T / C
gnomAD v2:
3-184045037-T-C
gnomAD v3:
3-184327249-T-C
gnomAD v4:
3-184327249-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184327249T>C , CM000665.2:g.184327249T>C | GRCh38 |
| NC_000003.11:g.184045037T>C , CM000665.1:g.184045037T>C | GRCh37 |
| NC_000003.10:g.185527731T>C | NCBI36 |
| NG_016850.1:g.17682T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000346169.7:c.3462T>C (EIF4G1) MANE Select | ENSP00000316879.5:p.Ala1154= | |
| ENST00000435046.7:c.3396T>C (EIF4G1) | ENSP00000404754.3:p.Ala1132= | |
| ENST00000676453.1:c.2809T>C (EIF4G1) | ENSP00000501695.1:n.2809T>C | |
| ENST00000319274.10:c.2868T>C (EIF4G1) | ENSP00000323737.7:p.Ala956= | |
| ENST00000342981.8:c.3465T>C (EIF4G1) | ENSP00000343450.4:p.Ala1155= | |
| ENST00000346169.6:c.3462T>C (EIF4G1) | ENSP00000316879.4:p.Ala1154= | |
| ENST00000350481.9:c.2970T>C (EIF4G1) | ENSP00000317600.8:p.Ala990= | |
| ENST00000352767.7:c.3483T>C (EIF4G1) | ENSP00000338020.4:p.Ala1161= | |
| ENST00000382330.7:c.3483T>C (EIF4G1) | ENSP00000371767.3:p.Ala1161= | |
| ENST00000392537.6:c.3201T>C (EIF4G1) | ENSP00000376320.2:p.Ala1067= | |
| ENST00000411531.5:c.3345T>C (EIF4G1) | ENSP00000395974.1:p.Ala1115= | |
| ENST00000414031.5:c.3342T>C (EIF4G1) | ENSP00000391935.1:p.Ala1114= | |
| ENST00000424196.5:c.3483T>C (EIF4G1) | ENSP00000416255.1:p.Ala1161= | |
| ENST00000427845.5:c.3204T>C (EIF4G1) | ENSP00000407682.1:p.Ala1068= | |
| ENST00000434061.6:c.2877T>C (EIF4G1) | ENSP00000411826.2:p.Ala959= | |
| ENST00000435046.6:c.2874T>C (EIF4G1) | ENSP00000404754.2:p.Ala958= | |
| ENST00000441154.5:c.2973T>C (EIF4G1) | ENSP00000399858.1:p.Ala991= | |
| ENST00000442406.5:c.*2901T>C (EIF4G1) | ENSP00000400351.1:n.*2901T>C | |
| ENST00000444495.1:c.2106+182542T>C (EIF2B5) | ENSP00000409142.1:n.2106+182542T>C | |
| ENST00000448284.1:c.623T>C (EIF4G1) | ||
| NM_001194946.1:c.3483T>C (EIF4G1) | NP_001181875.1:p.Ala1161= | |
| NM_001194947.1:c.3483T>C (EIF4G1) | NP_001181876.1:p.Ala1161= | |
| NM_001291157.1:c.3342T>C (EIF4G1) | NP_001278086.1:p.Ala1114= | |
| NM_004953.4:c.2877T>C (EIF4G1) | NP_004944.3:p.Ala959= | |
| NM_182917.4:c.3465T>C (EIF4G1) | NP_886553.3:p.Ala1155= | |
| NM_198241.2:c.3462T>C (EIF4G1) | NP_937884.1:p.Ala1154= | |
| NM_198242.2:c.2970T>C (EIF4G1) | NP_937885.1:p.Ala990= | |
| NM_198244.2:c.3201T>C (EIF4G1) | NP_937887.1:p.Ala1067= | |
| NM_001194946.2:c.3483T>C (EIF4G1) | NP_001181875.2:p.Ala1161= | |
| NM_001291157.2:c.3342T>C (EIF4G1) | NP_001278086.2:p.Ala1114= | |
| NM_004953.5:c.2877T>C (EIF4G1) | NP_004944.3:p.Ala959= | |
| NM_198241.3:c.3462T>C (EIF4G1) MANE Select | NP_937884.2:p.Ala1154= | |
| NM_198242.3:c.2970T>C (EIF4G1) | NP_937885.1:p.Ala990= | |
| NM_198244.3:c.3201T>C (EIF4G1) | NP_937887.2:p.Ala1067= | |
| NM_001194947.2:c.3483T>C (EIF4G1) | NP_001181876.2:p.Ala1161= |