Canonical Allele Identifier: CA355413036

Gene: EIF4G1 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184044681C>A (hg19) ; chr3:g.184326893C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184326893C>A , CM000665.2:g.184326893C>A	GRCh38
NC_000003.11:g.184044681C>A , CM000665.1:g.184044681C>A	GRCh37
NC_000003.10:g.185527375C>A	NCBI36
NG_016850.1:g.17326C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3338C>A (EIF4G1) MANE Select	ENSP00000316879.5:p.Ala1113Asp
ENST00000435046.7:c.3272C>A (EIF4G1)	ENSP00000404754.3:p.Ala1091Asp
ENST00000676453.1:c.2685C>A (EIF4G1)	ENSP00000501695.1:n.2685C>A
ENST00000319274.10:c.2744C>A (EIF4G1)	ENSP00000323737.7:p.Ala915Asp
ENST00000342981.8:c.3341C>A (EIF4G1)	ENSP00000343450.4:p.Ala1114Asp
ENST00000346169.6:c.3338C>A (EIF4G1)	ENSP00000316879.4:p.Ala1113Asp
ENST00000350481.9:c.2846C>A (EIF4G1)	ENSP00000317600.8:p.Ala949Asp
ENST00000352767.7:c.3359C>A (EIF4G1)	ENSP00000338020.4:p.Ala1120Asp
ENST00000382330.7:c.3359C>A (EIF4G1)	ENSP00000371767.3:p.Ala1120Asp
ENST00000392537.6:c.3077C>A (EIF4G1)	ENSP00000376320.2:p.Ala1026Asp
ENST00000411531.5:c.3221C>A (EIF4G1)	ENSP00000395974.1:p.Ala1074Asp
ENST00000414031.5:c.3218C>A (EIF4G1)	ENSP00000391935.1:p.Ala1073Asp
ENST00000424196.5:c.3359C>A (EIF4G1)	ENSP00000416255.1:p.Ala1120Asp
ENST00000427845.5:c.3080C>A (EIF4G1)	ENSP00000407682.1:p.Ala1027Asp
ENST00000434061.6:c.2753C>A (EIF4G1)	ENSP00000411826.2:p.Ala918Asp
ENST00000435046.6:c.2750C>A (EIF4G1)	ENSP00000404754.2:p.Ala917Asp
ENST00000441154.5:c.2849C>A (EIF4G1)	ENSP00000399858.1:p.Ala950Asp
ENST00000442406.5:c.*2777C>A (EIF4G1)	ENSP00000400351.1:n.*2777C>A
ENST00000444495.1:c.2106+182186C>A (EIF2B5)	ENSP00000409142.1:n.2106+182186C>A
ENST00000448284.1:c.499C>A (EIF4G1)
ENST00000466311.1:n.558C>A (EIF4G1)
NM_001194946.1:c.3359C>A (EIF4G1)	NP_001181875.1:p.Ala1120Asp
NM_001194947.1:c.3359C>A (EIF4G1)	NP_001181876.1:p.Ala1120Asp
NM_001291157.1:c.3218C>A (EIF4G1)	NP_001278086.1:p.Ala1073Asp
NM_004953.4:c.2753C>A (EIF4G1)	NP_004944.3:p.Ala918Asp
NM_182917.4:c.3341C>A (EIF4G1)	NP_886553.3:p.Ala1114Asp
NM_198241.2:c.3338C>A (EIF4G1)	NP_937884.1:p.Ala1113Asp
NM_198242.2:c.2846C>A (EIF4G1)	NP_937885.1:p.Ala949Asp
NM_198244.2:c.3077C>A (EIF4G1)	NP_937887.1:p.Ala1026Asp
NM_001194946.2:c.3359C>A (EIF4G1)	NP_001181875.2:p.Ala1120Asp
NM_001291157.2:c.3218C>A (EIF4G1)	NP_001278086.2:p.Ala1073Asp
NM_004953.5:c.2753C>A (EIF4G1)	NP_004944.3:p.Ala918Asp
NM_198241.3:c.3338C>A (EIF4G1) MANE Select	NP_937884.2:p.Ala1113Asp
NM_198242.3:c.2846C>A (EIF4G1)	NP_937885.1:p.Ala949Asp
NM_198244.3:c.3077C>A (EIF4G1)	NP_937887.2:p.Ala1026Asp
NM_001194947.2:c.3359C>A (EIF4G1)	NP_001181876.2:p.Ala1120Asp