Canonical Allele Identifier: CA355413042

Gene: EIF4G1 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184044683C>G (hg19) ; chr3:g.184326895C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184326895C>G , CM000665.2:g.184326895C>G	GRCh38
NC_000003.11:g.184044683C>G , CM000665.1:g.184044683C>G	GRCh37
NC_000003.10:g.185527377C>G	NCBI36
NG_016850.1:g.17328C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3340C>G (EIF4G1) MANE Select	ENSP00000316879.5:p.Arg1114Gly
ENST00000435046.7:c.3274C>G (EIF4G1)	ENSP00000404754.3:p.Arg1092Gly
ENST00000676453.1:c.2687C>G (EIF4G1)	ENSP00000501695.1:n.2687C>G
ENST00000319274.10:c.2746C>G (EIF4G1)	ENSP00000323737.7:p.Arg916Gly
ENST00000342981.8:c.3343C>G (EIF4G1)	ENSP00000343450.4:p.Arg1115Gly
ENST00000346169.6:c.3340C>G (EIF4G1)	ENSP00000316879.4:p.Arg1114Gly
ENST00000350481.9:c.2848C>G (EIF4G1)	ENSP00000317600.8:p.Arg950Gly
ENST00000352767.7:c.3361C>G (EIF4G1)	ENSP00000338020.4:p.Arg1121Gly
ENST00000382330.7:c.3361C>G (EIF4G1)	ENSP00000371767.3:p.Arg1121Gly
ENST00000392537.6:c.3079C>G (EIF4G1)	ENSP00000376320.2:p.Arg1027Gly
ENST00000411531.5:c.3223C>G (EIF4G1)	ENSP00000395974.1:p.Arg1075Gly
ENST00000414031.5:c.3220C>G (EIF4G1)	ENSP00000391935.1:p.Arg1074Gly
ENST00000424196.5:c.3361C>G (EIF4G1)	ENSP00000416255.1:p.Arg1121Gly
ENST00000427845.5:c.3082C>G (EIF4G1)	ENSP00000407682.1:p.Arg1028Gly
ENST00000434061.6:c.2755C>G (EIF4G1)	ENSP00000411826.2:p.Arg919Gly
ENST00000435046.6:c.2752C>G (EIF4G1)	ENSP00000404754.2:p.Arg918Gly
ENST00000441154.5:c.2851C>G (EIF4G1)	ENSP00000399858.1:p.Arg951Gly
ENST00000442406.5:c.*2779C>G (EIF4G1)	ENSP00000400351.1:n.*2779C>G
ENST00000444495.1:c.2106+182188C>G (EIF2B5)	ENSP00000409142.1:n.2106+182188C>G
ENST00000448284.1:c.501C>G (EIF4G1)
ENST00000466311.1:n.560C>G (EIF4G1)
NM_001194946.1:c.3361C>G (EIF4G1)	NP_001181875.1:p.Arg1121Gly
NM_001194947.1:c.3361C>G (EIF4G1)	NP_001181876.1:p.Arg1121Gly
NM_001291157.1:c.3220C>G (EIF4G1)	NP_001278086.1:p.Arg1074Gly
NM_004953.4:c.2755C>G (EIF4G1)	NP_004944.3:p.Arg919Gly
NM_182917.4:c.3343C>G (EIF4G1)	NP_886553.3:p.Arg1115Gly
NM_198241.2:c.3340C>G (EIF4G1)	NP_937884.1:p.Arg1114Gly
NM_198242.2:c.2848C>G (EIF4G1)	NP_937885.1:p.Arg950Gly
NM_198244.2:c.3079C>G (EIF4G1)	NP_937887.1:p.Arg1027Gly
NM_001194946.2:c.3361C>G (EIF4G1)	NP_001181875.2:p.Arg1121Gly
NM_001291157.2:c.3220C>G (EIF4G1)	NP_001278086.2:p.Arg1074Gly
NM_004953.5:c.2755C>G (EIF4G1)	NP_004944.3:p.Arg919Gly
NM_198241.3:c.3340C>G (EIF4G1) MANE Select	NP_937884.2:p.Arg1114Gly
NM_198242.3:c.2848C>G (EIF4G1)	NP_937885.1:p.Arg950Gly
NM_198244.3:c.3079C>G (EIF4G1)	NP_937887.2:p.Arg1027Gly
NM_001194947.2:c.3361C>G (EIF4G1)	NP_001181876.2:p.Arg1121Gly