Canonical Allele Identifier: CA2732827

Gene: EIF4G1 EIF2B5

Linked Data

• dbSNP Id: rs781494719
• ExAC: 3:184045071 C / T
• gnomAD v2: 3-184045071-C-T
• gnomAD v3: 3-184327283-C-T
• gnomAD v4: 3-184327283-C-T
• COSMIC: COSM5864038
• MyVariant Identifiers: chr3:g.184045071C>T (hg19) ; chr3:g.184327283C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184327283C>T , CM000665.2:g.184327283C>T	GRCh38
NC_000003.11:g.184045071C>T , CM000665.1:g.184045071C>T	GRCh37
NC_000003.10:g.185527765C>T	NCBI36
NG_016850.1:g.17716C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000346169.7:c.3496C>T (EIF4G1) MANE Select	ENSP00000316879.5:p.Arg1166Trp
ENST00000435046.7:c.3430C>T (EIF4G1)	ENSP00000404754.3:p.Arg1144Trp
ENST00000676453.1:c.2843C>T (EIF4G1)	ENSP00000501695.1:n.2843C>T
ENST00000319274.10:c.2901C>T (EIF4G1)	ENSP00000323737.7:p.Asn967=
ENST00000342981.8:c.3499C>T (EIF4G1)	ENSP00000343450.4:p.Arg1167Trp
ENST00000346169.6:c.3496C>T (EIF4G1)	ENSP00000316879.4:p.Arg1166Trp
ENST00000350481.9:c.3004C>T (EIF4G1)	ENSP00000317600.8:p.Arg1002Trp
ENST00000352767.7:c.3517C>T (EIF4G1)	ENSP00000338020.4:p.Arg1173Trp
ENST00000382330.7:c.3517C>T (EIF4G1)	ENSP00000371767.3:p.Arg1173Trp
ENST00000392537.6:c.3235C>T (EIF4G1)	ENSP00000376320.2:p.Arg1079Trp
ENST00000411531.5:c.3379C>T (EIF4G1)	ENSP00000395974.1:p.Arg1127Trp
ENST00000414031.5:c.3376C>T (EIF4G1)	ENSP00000391935.1:p.Arg1126Trp
ENST00000424196.5:c.3517C>T (EIF4G1)	ENSP00000416255.1:p.Arg1173Trp
ENST00000427845.5:c.3238C>T (EIF4G1)	ENSP00000407682.1:p.Arg1080Trp
ENST00000434061.6:c.2911C>T (EIF4G1)	ENSP00000411826.2:p.Arg971Trp
ENST00000435046.6:c.2908C>T (EIF4G1)	ENSP00000404754.2:p.Arg970Trp
ENST00000441154.5:c.3007C>T (EIF4G1)	ENSP00000399858.1:p.Arg1003Trp
ENST00000442406.5:c.*2935C>T (EIF4G1)	ENSP00000400351.1:n.*2935C>T
ENST00000444495.1:c.2106+182576C>T (EIF2B5)	ENSP00000409142.1:n.2106+182576C>T
ENST00000448284.1:c.657C>T (EIF4G1)
NM_001194946.1:c.3517C>T (EIF4G1)	NP_001181875.1:p.Arg1173Trp
NM_001194947.1:c.3517C>T (EIF4G1)	NP_001181876.1:p.Arg1173Trp
NM_001291157.1:c.3376C>T (EIF4G1)	NP_001278086.1:p.Arg1126Trp
NM_004953.4:c.2911C>T (EIF4G1)	NP_004944.3:p.Arg971Trp
NM_182917.4:c.3499C>T (EIF4G1)	NP_886553.3:p.Arg1167Trp
NM_198241.2:c.3496C>T (EIF4G1)	NP_937884.1:p.Arg1166Trp
NM_198242.2:c.3004C>T (EIF4G1)	NP_937885.1:p.Arg1002Trp
NM_198244.2:c.3235C>T (EIF4G1)	NP_937887.1:p.Arg1079Trp
NM_001194946.2:c.3517C>T (EIF4G1)	NP_001181875.2:p.Arg1173Trp
NM_001291157.2:c.3376C>T (EIF4G1)	NP_001278086.2:p.Arg1126Trp
NM_004953.5:c.2911C>T (EIF4G1)	NP_004944.3:p.Arg971Trp
NM_198241.3:c.3496C>T (EIF4G1) MANE Select	NP_937884.2:p.Arg1166Trp
NM_198242.3:c.3004C>T (EIF4G1)	NP_937885.1:p.Arg1002Trp
NM_198244.3:c.3235C>T (EIF4G1)	NP_937887.2:p.Arg1079Trp
NM_001194947.2:c.3517C>T (EIF4G1)	NP_001181876.2:p.Arg1173Trp