Canonical Allele Identifier: CA437162080

Gene: EIF4G1 EIF2B5

Linked Data

• dbSNP Id: rs2108503520
• MyVariant Identifiers: chr3:g.184044682T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184326894T>C , CM000665.2:g.184326894T>C	GRCh38
NC_000003.11:g.184044682T>C , CM000665.1:g.184044682T>C	GRCh37
NC_000003.10:g.185527376T>C	NCBI36
NG_016850.1:g.17327T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3339T>C (EIF4G1) MANE Select	ENSP00000316879.5:p.Ala1113=
ENST00000435046.7:c.3273T>C (EIF4G1)	ENSP00000404754.3:p.Ala1091=
ENST00000676453.1:c.2686T>C (EIF4G1)	ENSP00000501695.1:n.2686T>C
ENST00000319274.10:c.2745T>C (EIF4G1)	ENSP00000323737.7:p.Ala915=
ENST00000342981.8:c.3342T>C (EIF4G1)	ENSP00000343450.4:p.Ala1114=
ENST00000346169.6:c.3339T>C (EIF4G1)	ENSP00000316879.4:p.Ala1113=
ENST00000350481.9:c.2847T>C (EIF4G1)	ENSP00000317600.8:p.Ala949=
ENST00000352767.7:c.3360T>C (EIF4G1)	ENSP00000338020.4:p.Ala1120=
ENST00000382330.7:c.3360T>C (EIF4G1)	ENSP00000371767.3:p.Ala1120=
ENST00000392537.6:c.3078T>C (EIF4G1)	ENSP00000376320.2:p.Ala1026=
ENST00000411531.5:c.3222T>C (EIF4G1)	ENSP00000395974.1:p.Ala1074=
ENST00000414031.5:c.3219T>C (EIF4G1)	ENSP00000391935.1:p.Ala1073=
ENST00000424196.5:c.3360T>C (EIF4G1)	ENSP00000416255.1:p.Ala1120=
ENST00000427845.5:c.3081T>C (EIF4G1)	ENSP00000407682.1:p.Ala1027=
ENST00000434061.6:c.2754T>C (EIF4G1)	ENSP00000411826.2:p.Ala918=
ENST00000435046.6:c.2751T>C (EIF4G1)	ENSP00000404754.2:p.Ala917=
ENST00000441154.5:c.2850T>C (EIF4G1)	ENSP00000399858.1:p.Ala950=
ENST00000442406.5:c.*2778T>C (EIF4G1)	ENSP00000400351.1:n.*2778T>C
ENST00000444495.1:c.2106+182187T>C (EIF2B5)	ENSP00000409142.1:n.2106+182187T>C
ENST00000448284.1:c.500T>C (EIF4G1)
ENST00000466311.1:n.559T>C (EIF4G1)
NM_001194946.1:c.3360T>C (EIF4G1)	NP_001181875.1:p.Ala1120=
NM_001194947.1:c.3360T>C (EIF4G1)	NP_001181876.1:p.Ala1120=
NM_001291157.1:c.3219T>C (EIF4G1)	NP_001278086.1:p.Ala1073=
NM_004953.4:c.2754T>C (EIF4G1)	NP_004944.3:p.Ala918=
NM_182917.4:c.3342T>C (EIF4G1)	NP_886553.3:p.Ala1114=
NM_198241.2:c.3339T>C (EIF4G1)	NP_937884.1:p.Ala1113=
NM_198242.2:c.2847T>C (EIF4G1)	NP_937885.1:p.Ala949=
NM_198244.2:c.3078T>C (EIF4G1)	NP_937887.1:p.Ala1026=
NM_001194946.2:c.3360T>C (EIF4G1)	NP_001181875.2:p.Ala1120=
NM_001291157.2:c.3219T>C (EIF4G1)	NP_001278086.2:p.Ala1073=
NM_004953.5:c.2754T>C (EIF4G1)	NP_004944.3:p.Ala918=
NM_198241.3:c.3339T>C (EIF4G1) MANE Select	NP_937884.2:p.Ala1113=
NM_198242.3:c.2847T>C (EIF4G1)	NP_937885.1:p.Ala949=
NM_198244.3:c.3078T>C (EIF4G1)	NP_937887.2:p.Ala1026=
NM_001194947.2:c.3360T>C (EIF4G1)	NP_001181876.2:p.Ala1120=