Canonical Allele Identifier: CA355415204

Gene: EIF4G1 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184045173C>T (hg19) ; chr3:g.184327385C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184327385C>T , CM000665.2:g.184327385C>T	GRCh38
NC_000003.11:g.184045173C>T , CM000665.1:g.184045173C>T	GRCh37
NC_000003.10:g.185527867C>T	NCBI36
NG_016850.1:g.17818C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000346169.7:c.3598C>T (EIF4G1) MANE Select	ENSP00000316879.5:p.Gln1200Ter
ENST00000435046.7:c.3532C>T (EIF4G1)	ENSP00000404754.3:p.Gln1178Ter
ENST00000676453.1:c.2945C>T (EIF4G1)	ENSP00000501695.1:n.2945C>T
ENST00000319274.10:c.3001C>T (EIF4G1)	ENSP00000323737.7:p.Gln1001Ter
ENST00000342981.8:c.3601C>T (EIF4G1)	ENSP00000343450.4:p.Gln1201Ter
ENST00000346169.6:c.3598C>T (EIF4G1)	ENSP00000316879.4:p.Gln1200Ter
ENST00000350481.9:c.3106C>T (EIF4G1)	ENSP00000317600.8:p.Gln1036Ter
ENST00000352767.7:c.3619C>T (EIF4G1)	ENSP00000338020.4:p.Gln1207Ter
ENST00000382330.7:c.3619C>T (EIF4G1)	ENSP00000371767.3:p.Gln1207Ter
ENST00000392537.6:c.3337C>T (EIF4G1)	ENSP00000376320.2:p.Gln1113Ter
ENST00000411531.5:c.3481C>T (EIF4G1)	ENSP00000395974.1:p.Gln1161Ter
ENST00000414031.5:c.3478C>T (EIF4G1)	ENSP00000391935.1:p.Gln1160Ter
ENST00000424196.5:c.3619C>T (EIF4G1)	ENSP00000416255.1:p.Gln1207Ter
ENST00000427845.5:c.3340C>T (EIF4G1)	ENSP00000407682.1:p.Gln1114Ter
ENST00000434061.6:c.3013C>T (EIF4G1)	ENSP00000411826.2:p.Gln1005Ter
ENST00000435046.6:c.3010C>T (EIF4G1)	ENSP00000404754.2:p.Gln1004Ter
ENST00000441154.5:c.3109C>T (EIF4G1)	ENSP00000399858.1:p.Gln1037Ter
ENST00000442406.5:c.*3037C>T (EIF4G1)	ENSP00000400351.1:n.*3037C>T
ENST00000444495.1:c.2106+182678C>T (EIF2B5)	ENSP00000409142.1:n.2106+182678C>T
ENST00000482303.1:n.100C>T (EIF4G1)
NM_001194946.1:c.3619C>T (EIF4G1)	NP_001181875.1:p.Gln1207Ter
NM_001194947.1:c.3619C>T (EIF4G1)	NP_001181876.1:p.Gln1207Ter
NM_001291157.1:c.3478C>T (EIF4G1)	NP_001278086.1:p.Gln1160Ter
NM_004953.4:c.3013C>T (EIF4G1)	NP_004944.3:p.Gln1005Ter
NM_182917.4:c.3601C>T (EIF4G1)	NP_886553.3:p.Gln1201Ter
NM_198241.2:c.3598C>T (EIF4G1)	NP_937884.1:p.Gln1200Ter
NM_198242.2:c.3106C>T (EIF4G1)	NP_937885.1:p.Gln1036Ter
NM_198244.2:c.3337C>T (EIF4G1)	NP_937887.1:p.Gln1113Ter
NM_001194946.2:c.3619C>T (EIF4G1)	NP_001181875.2:p.Gln1207Ter
NM_001291157.2:c.3478C>T (EIF4G1)	NP_001278086.2:p.Gln1160Ter
NM_004953.5:c.3013C>T (EIF4G1)	NP_004944.3:p.Gln1005Ter
NM_198241.3:c.3598C>T (EIF4G1) MANE Select	NP_937884.2:p.Gln1200Ter
NM_198242.3:c.3106C>T (EIF4G1)	NP_937885.1:p.Gln1036Ter
NM_198244.3:c.3337C>T (EIF4G1)	NP_937887.2:p.Gln1113Ter
NM_001194947.2:c.3619C>T (EIF4G1)	NP_001181876.2:p.Gln1207Ter