Linked Data
dbSNP Id:
rs879238199
MyVariant Identifiers:
chr3:g.184044995_184044996insTCTC (hg19)
chr3:g.184327207_184327208insTCTC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.184327210_184327211insCTCT , CM000665.2:g.184327210_184327211insCTCT | GRCh38 |
| NC_000003.11:g.184044998_184044999insCTCT , CM000665.1:g.184044998_184044999insCTCT | GRCh37 |
| NC_000003.10:g.185527692_185527693insCTCT | NCBI36 |
| NG_016850.1:g.17643_17644insCTCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000346169.7:c.3429-6_3429-5insCTCT (EIF4G1) MANE Select | ENSP00000316879.5:n.3429-6_3429-5insCTCT | |
| ENST00000435046.7:c.3363-6_3363-5insCTCT (EIF4G1) | ENSP00000404754.3:n.3363-6_3363-5insCTCT | |
| ENST00000676453.1:c.2776-6_2776-5insCTCT (EIF4G1) | ENSP00000501695.1:n.2776-6_2776-5insCTCT | |
| ENST00000319274.10:c.2835-6_2835-5insCTCT (EIF4G1) | ENSP00000323737.7:n.2835-6_2835-5insCTCT | |
| ENST00000342981.8:c.3432-6_3432-5insCTCT (EIF4G1) | ENSP00000343450.4:n.3432-6_3432-5insCTCT | |
| ENST00000346169.6:c.3429-6_3429-5insCTCT (EIF4G1) | ENSP00000316879.4:n.3429-6_3429-5insCTCT | |
| ENST00000350481.9:c.2937-6_2937-5insCTCT (EIF4G1) | ENSP00000317600.8:n.2937-6_2937-5insCTCT | |
| ENST00000352767.7:c.3450-6_3450-5insCTCT (EIF4G1) | ENSP00000338020.4:n.3450-6_3450-5insCTCT | |
| ENST00000382330.7:c.3450-6_3450-5insCTCT (EIF4G1) | ENSP00000371767.3:n.3450-6_3450-5insCTCT | |
| ENST00000392537.6:c.3168-6_3168-5insCTCT (EIF4G1) | ENSP00000376320.2:n.3168-6_3168-5insCTCT | |
| ENST00000411531.5:c.3312-6_3312-5insCTCT (EIF4G1) | ENSP00000395974.1:n.3312-6_3312-5insCTCT | |
| ENST00000414031.5:c.3309-6_3309-5insCTCT (EIF4G1) | ENSP00000391935.1:n.3309-6_3309-5insCTCT | |
| ENST00000424196.5:c.3450-6_3450-5insCTCT (EIF4G1) | ENSP00000416255.1:n.3450-6_3450-5insCTCT | |
| ENST00000427845.5:c.3171-6_3171-5insCTCT (EIF4G1) | ENSP00000407682.1:n.3171-6_3171-5insCTCT | |
| ENST00000434061.6:c.2844-6_2844-5insCTCT (EIF4G1) | ENSP00000411826.2:n.2844-6_2844-5insCTCT | |
| ENST00000435046.6:c.2841-6_2841-5insCTCT (EIF4G1) | ENSP00000404754.2:n.2841-6_2841-5insCTCT | |
| ENST00000441154.5:c.2940-6_2940-5insCTCT (EIF4G1) | ENSP00000399858.1:n.2940-6_2940-5insCTCT | |
| ENST00000442406.5:c.*2868-6_*2868-5insCTCT (EIF4G1) | ENSP00000400351.1:n.*2868-6_*2868-5insCTCT | |
| ENST00000444495.1:c.2106+182503_2106+182504insCTCT (EIF2B5) | ENSP00000409142.1:n.2106+182503_2106+182504insCTCT | |
| ENST00000448284.1:c.590-6_590-5insCTCT (EIF4G1) | ||
| NM_001194946.1:c.3450-6_3450-5insCTCT (EIF4G1) | NP_001181875.1:n.3450-6_3450-5insCTCT | |
| NM_001194947.1:c.3450-6_3450-5insCTCT (EIF4G1) | NP_001181876.1:n.3450-6_3450-5insCTCT | |
| NM_001291157.1:c.3309-6_3309-5insCTCT (EIF4G1) | NP_001278086.1:n.3309-6_3309-5insCTCT | |
| NM_004953.4:c.2844-6_2844-5insCTCT (EIF4G1) | NP_004944.3:n.2844-6_2844-5insCTCT | |
| NM_182917.4:c.3432-6_3432-5insCTCT (EIF4G1) | NP_886553.3:n.3432-6_3432-5insCTCT | |
| NM_198241.2:c.3429-6_3429-5insCTCT (EIF4G1) | NP_937884.1:n.3429-6_3429-5insCTCT | |
| NM_198242.2:c.2937-6_2937-5insCTCT (EIF4G1) | NP_937885.1:n.2937-6_2937-5insCTCT | |
| NM_198244.2:c.3168-6_3168-5insCTCT (EIF4G1) | NP_937887.1:n.3168-6_3168-5insCTCT | |
| NM_001194946.2:c.3450-6_3450-5insCTCT (EIF4G1) | NP_001181875.2:n.3450-6_3450-5insCTCT | |
| NM_001291157.2:c.3309-6_3309-5insCTCT (EIF4G1) | NP_001278086.2:n.3309-6_3309-5insCTCT | |
| NM_004953.5:c.2844-6_2844-5insCTCT (EIF4G1) | NP_004944.3:n.2844-6_2844-5insCTCT | |
| NM_198241.3:c.3429-6_3429-5insCTCT (EIF4G1) MANE Select | NP_937884.2:n.3429-6_3429-5insCTCT | |
| NM_198242.3:c.2937-6_2937-5insCTCT (EIF4G1) | NP_937885.1:n.2937-6_2937-5insCTCT | |
| NM_198244.3:c.3168-6_3168-5insCTCT (EIF4G1) | NP_937887.2:n.3168-6_3168-5insCTCT | |
| NM_001194947.2:c.3450-6_3450-5insCTCT (EIF4G1) | NP_001181876.2:n.3450-6_3450-5insCTCT |