Canonical Allele Identifier: CA88867229

Gene: EIF4G1 EIF2B5

Linked Data

• dbSNP Id: rs532220949
• gnomAD v4: 3-184326904-A-G
• COSMIC: COSM232240
• MyVariant Identifiers: chr3:g.184044692A>G (hg19) ; chr3:g.184326904A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184326904A>G , CM000665.2:g.184326904A>G	GRCh38
NC_000003.11:g.184044692A>G , CM000665.1:g.184044692A>G	GRCh37
NC_000003.10:g.185527386A>G	NCBI36
NG_016850.1:g.17337A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3349A>G (EIF4G1) MANE Select	ENSP00000316879.5:p.Thr1117Ala
ENST00000435046.7:c.3283A>G (EIF4G1)	ENSP00000404754.3:p.Thr1095Ala
ENST00000676453.1:c.2696A>G (EIF4G1)	ENSP00000501695.1:n.2696A>G
ENST00000319274.10:c.2755A>G (EIF4G1)	ENSP00000323737.7:p.Thr919Ala
ENST00000342981.8:c.3352A>G (EIF4G1)	ENSP00000343450.4:p.Thr1118Ala
ENST00000346169.6:c.3349A>G (EIF4G1)	ENSP00000316879.4:p.Thr1117Ala
ENST00000350481.9:c.2857A>G (EIF4G1)	ENSP00000317600.8:p.Thr953Ala
ENST00000352767.7:c.3370A>G (EIF4G1)	ENSP00000338020.4:p.Thr1124Ala
ENST00000382330.7:c.3370A>G (EIF4G1)	ENSP00000371767.3:p.Thr1124Ala
ENST00000392537.6:c.3088A>G (EIF4G1)	ENSP00000376320.2:p.Thr1030Ala
ENST00000411531.5:c.3232A>G (EIF4G1)	ENSP00000395974.1:p.Thr1078Ala
ENST00000414031.5:c.3229A>G (EIF4G1)	ENSP00000391935.1:p.Thr1077Ala
ENST00000424196.5:c.3370A>G (EIF4G1)	ENSP00000416255.1:p.Thr1124Ala
ENST00000427845.5:c.3091A>G (EIF4G1)	ENSP00000407682.1:p.Thr1031Ala
ENST00000434061.6:c.2764A>G (EIF4G1)	ENSP00000411826.2:p.Thr922Ala
ENST00000435046.6:c.2761A>G (EIF4G1)	ENSP00000404754.2:p.Thr921Ala
ENST00000441154.5:c.2860A>G (EIF4G1)	ENSP00000399858.1:p.Thr954Ala
ENST00000442406.5:c.*2788A>G (EIF4G1)	ENSP00000400351.1:n.*2788A>G
ENST00000444495.1:c.2106+182197A>G (EIF2B5)	ENSP00000409142.1:n.2106+182197A>G
ENST00000448284.1:c.510A>G (EIF4G1)
ENST00000466311.1:n.569A>G (EIF4G1)
NM_001194946.1:c.3370A>G (EIF4G1)	NP_001181875.1:p.Thr1124Ala
NM_001194947.1:c.3370A>G (EIF4G1)	NP_001181876.1:p.Thr1124Ala
NM_001291157.1:c.3229A>G (EIF4G1)	NP_001278086.1:p.Thr1077Ala
NM_004953.4:c.2764A>G (EIF4G1)	NP_004944.3:p.Thr922Ala
NM_182917.4:c.3352A>G (EIF4G1)	NP_886553.3:p.Thr1118Ala
NM_198241.2:c.3349A>G (EIF4G1)	NP_937884.1:p.Thr1117Ala
NM_198242.2:c.2857A>G (EIF4G1)	NP_937885.1:p.Thr953Ala
NM_198244.2:c.3088A>G (EIF4G1)	NP_937887.1:p.Thr1030Ala
NM_001194946.2:c.3370A>G (EIF4G1)	NP_001181875.2:p.Thr1124Ala
NM_001291157.2:c.3229A>G (EIF4G1)	NP_001278086.2:p.Thr1077Ala
NM_004953.5:c.2764A>G (EIF4G1)	NP_004944.3:p.Thr922Ala
NM_198241.3:c.3349A>G (EIF4G1) MANE Select	NP_937884.2:p.Thr1117Ala
NM_198242.3:c.2857A>G (EIF4G1)	NP_937885.1:p.Thr953Ala
NM_198244.3:c.3088A>G (EIF4G1)	NP_937887.2:p.Thr1030Ala
NM_001194947.2:c.3370A>G (EIF4G1)	NP_001181876.2:p.Thr1124Ala