Canonical Allele Identifier: CA88863405

Gene: EIF4G1 EIF2B5

Linked Data

• dbSNP Id: rs953496082
• gnomAD v2: 3-184039767-A-T
• gnomAD v4: 3-184321979-A-T
• MyVariant Identifiers: chr3:g.184039767A>T (hg19) ; chr3:g.184321979A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184321979A>T , CM000665.2:g.184321979A>T	GRCh38
NC_000003.11:g.184039767A>T , CM000665.1:g.184039767A>T	GRCh37
NC_000003.10:g.185522461A>T	NCBI36
NG_016850.1:g.12412A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.1395A>T (EIF4G1) MANE Select	ENSP00000316879.5:p.Glu465Asp
ENST00000435046.7:c.1329A>T (EIF4G1)	ENSP00000404754.3:p.Glu443Asp
ENST00000676453.1:c.765A>T (EIF4G1)	ENSP00000501695.1:p.Glu255Asp
ENST00000319274.10:c.807A>T (EIF4G1)	ENSP00000323737.7:p.Glu269Asp
ENST00000342981.8:c.1395A>T (EIF4G1)	ENSP00000343450.4:p.Glu465Asp
ENST00000346169.6:c.1395A>T (EIF4G1)	ENSP00000316879.4:p.Glu465Asp
ENST00000350481.9:c.903A>T (EIF4G1)	ENSP00000317600.8:p.Glu301Asp
ENST00000352767.7:c.1416A>T (EIF4G1)	ENSP00000338020.4:p.Glu472Asp
ENST00000382330.7:c.1416A>T (EIF4G1)	ENSP00000371767.3:p.Glu472Asp
ENST00000392537.6:c.1134A>T (EIF4G1)	ENSP00000376320.2:p.Glu378Asp
ENST00000411531.5:c.1275A>T (EIF4G1)	ENSP00000395974.1:p.Glu425Asp
ENST00000413967.5:c.*902A>T (EIF4G1)	ENSP00000390755.1:n.*902A>T
ENST00000414031.5:c.1275A>T (EIF4G1)	ENSP00000391935.1:p.Glu425Asp
ENST00000421110.5:c.1416A>T (EIF4G1)	ENSP00000413159.1:p.Glu472Asp
ENST00000424196.5:c.1416A>T (EIF4G1)	ENSP00000416255.1:p.Glu472Asp
ENST00000426123.5:c.1218A>T (EIF4G1)	ENSP00000403269.1:p.Glu406Asp
ENST00000427845.5:c.1134A>T (EIF4G1)	ENSP00000407682.1:p.Glu378Asp
ENST00000434061.6:c.807A>T (EIF4G1)	ENSP00000411826.2:p.Glu269Asp
ENST00000435046.6:c.807A>T (EIF4G1)	ENSP00000404754.2:p.Glu269Asp
ENST00000441154.5:c.903A>T (EIF4G1)	ENSP00000399858.1:p.Glu301Asp
ENST00000442406.5:c.*834A>T (EIF4G1)	ENSP00000400351.1:n.*834A>T
ENST00000444495.1:c.2106+177272A>T (EIF2B5)	ENSP00000409142.1:n.2106+177272A>T
ENST00000444861.5:c.903A>T (EIF4G1)	ENSP00000398145.1:p.Glu301Asp
ENST00000450424.5:c.1395A>T (EIF4G1)	ENSP00000391412.1:p.Glu465Asp
ENST00000457456.5:c.807A>T (EIF4G1)	ENSP00000399969.1:p.Glu269Asp
NM_001194946.1:c.1416A>T (EIF4G1)	NP_001181875.1:p.Glu472Asp
NM_001194947.1:c.1416A>T (EIF4G1)	NP_001181876.1:p.Glu472Asp
NM_001291157.1:c.1275A>T (EIF4G1)	NP_001278086.1:p.Glu425Asp
NM_004953.4:c.807A>T (EIF4G1)	NP_004944.3:p.Glu269Asp
NM_182917.4:c.1395A>T (EIF4G1)	NP_886553.3:p.Glu465Asp
NM_198241.2:c.1395A>T (EIF4G1)	NP_937884.1:p.Glu465Asp
NM_198242.2:c.903A>T (EIF4G1)	NP_937885.1:p.Glu301Asp
NM_198244.2:c.1134A>T (EIF4G1)	NP_937887.1:p.Glu378Asp
NM_001194946.2:c.1416A>T (EIF4G1)	NP_001181875.2:p.Glu472Asp
NM_001291157.2:c.1275A>T (EIF4G1)	NP_001278086.2:p.Glu425Asp
NM_004953.5:c.807A>T (EIF4G1)	NP_004944.3:p.Glu269Asp
NM_198241.3:c.1395A>T (EIF4G1) MANE Select	NP_937884.2:p.Glu465Asp
NM_198242.3:c.903A>T (EIF4G1)	NP_937885.1:p.Glu301Asp
NM_198244.3:c.1134A>T (EIF4G1)	NP_937887.2:p.Glu378Asp
NM_001194947.2:c.1416A>T (EIF4G1)	NP_001181876.2:p.Glu472Asp