Canonical Allele Identifier: CA437162095

Gene: EIF4G1 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184044700T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184326912T>A , CM000665.2:g.184326912T>A	GRCh38
NC_000003.11:g.184044700T>A , CM000665.1:g.184044700T>A	GRCh37
NC_000003.10:g.185527394T>A	NCBI36
NG_016850.1:g.17345T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3357T>A (EIF4G1) MANE Select	ENSP00000316879.5:p.Thr1119=
ENST00000435046.7:c.3291T>A (EIF4G1)	ENSP00000404754.3:p.Thr1097=
ENST00000676453.1:c.2704T>A (EIF4G1)	ENSP00000501695.1:n.2704T>A
ENST00000319274.10:c.2763T>A (EIF4G1)	ENSP00000323737.7:p.Thr921=
ENST00000342981.8:c.3360T>A (EIF4G1)	ENSP00000343450.4:p.Thr1120=
ENST00000346169.6:c.3357T>A (EIF4G1)	ENSP00000316879.4:p.Thr1119=
ENST00000350481.9:c.2865T>A (EIF4G1)	ENSP00000317600.8:p.Thr955=
ENST00000352767.7:c.3378T>A (EIF4G1)	ENSP00000338020.4:p.Thr1126=
ENST00000382330.7:c.3378T>A (EIF4G1)	ENSP00000371767.3:p.Thr1126=
ENST00000392537.6:c.3096T>A (EIF4G1)	ENSP00000376320.2:p.Thr1032=
ENST00000411531.5:c.3240T>A (EIF4G1)	ENSP00000395974.1:p.Thr1080=
ENST00000414031.5:c.3237T>A (EIF4G1)	ENSP00000391935.1:p.Thr1079=
ENST00000424196.5:c.3378T>A (EIF4G1)	ENSP00000416255.1:p.Thr1126=
ENST00000427845.5:c.3099T>A (EIF4G1)	ENSP00000407682.1:p.Thr1033=
ENST00000434061.6:c.2772T>A (EIF4G1)	ENSP00000411826.2:p.Thr924=
ENST00000435046.6:c.2769T>A (EIF4G1)	ENSP00000404754.2:p.Thr923=
ENST00000441154.5:c.2868T>A (EIF4G1)	ENSP00000399858.1:p.Thr956=
ENST00000442406.5:c.*2796T>A (EIF4G1)	ENSP00000400351.1:n.*2796T>A
ENST00000444495.1:c.2106+182205T>A (EIF2B5)	ENSP00000409142.1:n.2106+182205T>A
ENST00000448284.1:c.518T>A (EIF4G1)
NM_001194946.1:c.3378T>A (EIF4G1)	NP_001181875.1:p.Thr1126=
NM_001194947.1:c.3378T>A (EIF4G1)	NP_001181876.1:p.Thr1126=
NM_001291157.1:c.3237T>A (EIF4G1)	NP_001278086.1:p.Thr1079=
NM_004953.4:c.2772T>A (EIF4G1)	NP_004944.3:p.Thr924=
NM_182917.4:c.3360T>A (EIF4G1)	NP_886553.3:p.Thr1120=
NM_198241.2:c.3357T>A (EIF4G1)	NP_937884.1:p.Thr1119=
NM_198242.2:c.2865T>A (EIF4G1)	NP_937885.1:p.Thr955=
NM_198244.2:c.3096T>A (EIF4G1)	NP_937887.1:p.Thr1032=
NM_001194946.2:c.3378T>A (EIF4G1)	NP_001181875.2:p.Thr1126=
NM_001291157.2:c.3237T>A (EIF4G1)	NP_001278086.2:p.Thr1079=
NM_004953.5:c.2772T>A (EIF4G1)	NP_004944.3:p.Thr924=
NM_198241.3:c.3357T>A (EIF4G1) MANE Select	NP_937884.2:p.Thr1119=
NM_198242.3:c.2865T>A (EIF4G1)	NP_937885.1:p.Thr955=
NM_198244.3:c.3096T>A (EIF4G1)	NP_937887.2:p.Thr1032=
NM_001194947.2:c.3378T>A (EIF4G1)	NP_001181876.2:p.Thr1126=