Canonical Allele Identifier: CA355414136

Gene: EIF4G1 EIF2B5

Linked Data

• dbSNP Id: rs1425712161
• gnomAD v2: 3-184045053-C-T
• gnomAD v4: 3-184327265-C-T
• MyVariant Identifiers: chr3:g.184045053C>T (hg19) ; chr3:g.184327265C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184327265C>T , CM000665.2:g.184327265C>T	GRCh38
NC_000003.11:g.184045053C>T , CM000665.1:g.184045053C>T	GRCh37
NC_000003.10:g.185527747C>T	NCBI36
NG_016850.1:g.17698C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3478C>T (EIF4G1) MANE Select	ENSP00000316879.5:p.Arg1160Cys
ENST00000435046.7:c.3412C>T (EIF4G1)	ENSP00000404754.3:p.Arg1138Cys
ENST00000676453.1:c.2825C>T (EIF4G1)	ENSP00000501695.1:n.2825C>T
ENST00000319274.10:c.2884C>T (EIF4G1)	ENSP00000323737.7:p.Arg962Cys
ENST00000342981.8:c.3481C>T (EIF4G1)	ENSP00000343450.4:p.Arg1161Cys
ENST00000346169.6:c.3478C>T (EIF4G1)	ENSP00000316879.4:p.Arg1160Cys
ENST00000350481.9:c.2986C>T (EIF4G1)	ENSP00000317600.8:p.Arg996Cys
ENST00000352767.7:c.3499C>T (EIF4G1)	ENSP00000338020.4:p.Arg1167Cys
ENST00000382330.7:c.3499C>T (EIF4G1)	ENSP00000371767.3:p.Arg1167Cys
ENST00000392537.6:c.3217C>T (EIF4G1)	ENSP00000376320.2:p.Arg1073Cys
ENST00000411531.5:c.3361C>T (EIF4G1)	ENSP00000395974.1:p.Arg1121Cys
ENST00000414031.5:c.3358C>T (EIF4G1)	ENSP00000391935.1:p.Arg1120Cys
ENST00000424196.5:c.3499C>T (EIF4G1)	ENSP00000416255.1:p.Arg1167Cys
ENST00000427845.5:c.3220C>T (EIF4G1)	ENSP00000407682.1:p.Arg1074Cys
ENST00000434061.6:c.2893C>T (EIF4G1)	ENSP00000411826.2:p.Arg965Cys
ENST00000435046.6:c.2890C>T (EIF4G1)	ENSP00000404754.2:p.Arg964Cys
ENST00000441154.5:c.2989C>T (EIF4G1)	ENSP00000399858.1:p.Arg997Cys
ENST00000442406.5:c.*2917C>T (EIF4G1)	ENSP00000400351.1:n.*2917C>T
ENST00000444495.1:c.2106+182558C>T (EIF2B5)	ENSP00000409142.1:n.2106+182558C>T
ENST00000448284.1:c.639C>T (EIF4G1)
NM_001194946.1:c.3499C>T (EIF4G1)	NP_001181875.1:p.Arg1167Cys
NM_001194947.1:c.3499C>T (EIF4G1)	NP_001181876.1:p.Arg1167Cys
NM_001291157.1:c.3358C>T (EIF4G1)	NP_001278086.1:p.Arg1120Cys
NM_004953.4:c.2893C>T (EIF4G1)	NP_004944.3:p.Arg965Cys
NM_182917.4:c.3481C>T (EIF4G1)	NP_886553.3:p.Arg1161Cys
NM_198241.2:c.3478C>T (EIF4G1)	NP_937884.1:p.Arg1160Cys
NM_198242.2:c.2986C>T (EIF4G1)	NP_937885.1:p.Arg996Cys
NM_198244.2:c.3217C>T (EIF4G1)	NP_937887.1:p.Arg1073Cys
NM_001194946.2:c.3499C>T (EIF4G1)	NP_001181875.2:p.Arg1167Cys
NM_001291157.2:c.3358C>T (EIF4G1)	NP_001278086.2:p.Arg1120Cys
NM_004953.5:c.2893C>T (EIF4G1)	NP_004944.3:p.Arg965Cys
NM_198241.3:c.3478C>T (EIF4G1) MANE Select	NP_937884.2:p.Arg1160Cys
NM_198242.3:c.2986C>T (EIF4G1)	NP_937885.1:p.Arg996Cys
NM_198244.3:c.3217C>T (EIF4G1)	NP_937887.2:p.Arg1073Cys
NM_001194947.2:c.3499C>T (EIF4G1)	NP_001181876.2:p.Arg1167Cys