Canonical Allele Identifier: CA1425957832

Gene: EIF4G1 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184326966T= , CM000665.2:g.184326966T=	GRCh38
NC_000003.11:g.184044754T= , CM000665.1:g.184044754T=	GRCh37
NC_000003.10:g.185527448T=	NCBI36
NG_016850.1:g.17399T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3411T= (EIF4G1) MANE Select	ENSP00000316879.5:p.Asn1137=
ENST00000435046.7:c.3345T= (EIF4G1)	ENSP00000404754.3:p.Asn1115=
ENST00000676453.1:c.2758T= (EIF4G1)	ENSP00000501695.1:n.2758T=
ENST00000319274.10:c.2817T= (EIF4G1)	ENSP00000323737.7:p.Asn939=
ENST00000342981.8:c.3414T= (EIF4G1)	ENSP00000343450.4:p.Asn1138=
ENST00000346169.6:c.3411T= (EIF4G1)	ENSP00000316879.4:p.Asn1137=
ENST00000350481.9:c.2919T= (EIF4G1)	ENSP00000317600.8:p.Asn973=
ENST00000352767.7:c.3432T= (EIF4G1)	ENSP00000338020.4:p.Asn1144=
ENST00000382330.7:c.3432T= (EIF4G1)	ENSP00000371767.3:p.Asn1144=
ENST00000392537.6:c.3150T= (EIF4G1)	ENSP00000376320.2:p.Asn1050=
ENST00000411531.5:c.3294T= (EIF4G1)	ENSP00000395974.1:p.Asn1098=
ENST00000414031.5:c.3291T= (EIF4G1)	ENSP00000391935.1:p.Asn1097=
ENST00000424196.5:c.3432T= (EIF4G1)	ENSP00000416255.1:p.Asn1144=
ENST00000427845.5:c.3153T= (EIF4G1)	ENSP00000407682.1:p.Asn1051=
ENST00000434061.6:c.2826T= (EIF4G1)	ENSP00000411826.2:p.Asn942=
ENST00000435046.6:c.2823T= (EIF4G1)	ENSP00000404754.2:p.Asn941=
ENST00000441154.5:c.2922T= (EIF4G1)	ENSP00000399858.1:p.Asn974=
ENST00000442406.5:c.*2850T= (EIF4G1)	ENSP00000400351.1:n.*2850T=
ENST00000444495.1:c.2106+182259T= (EIF2B5)	ENSP00000409142.1:n.2106+182259T=
ENST00000448284.1:c.572T= (EIF4G1)
NM_001194946.1:c.3432T= (EIF4G1)	NP_001181875.1:p.Asn1144=
NM_001194947.1:c.3432T= (EIF4G1)	NP_001181876.1:p.Asn1144=
NM_001291157.1:c.3291T= (EIF4G1)	NP_001278086.1:p.Asn1097=
NM_004953.4:c.2826T= (EIF4G1)	NP_004944.3:p.Asn942=
NM_182917.4:c.3414T= (EIF4G1)	NP_886553.3:p.Asn1138=
NM_198241.2:c.3411T= (EIF4G1)	NP_937884.1:p.Asn1137=
NM_198242.2:c.2919T= (EIF4G1)	NP_937885.1:p.Asn973=
NM_198244.2:c.3150T= (EIF4G1)	NP_937887.1:p.Asn1050=
NM_001194946.2:c.3432T= (EIF4G1)	NP_001181875.2:p.Asn1144=
NM_001291157.2:c.3291T= (EIF4G1)	NP_001278086.2:p.Asn1097=
NM_004953.5:c.2826T= (EIF4G1)	NP_004944.3:p.Asn942=
NM_198241.3:c.3411T= (EIF4G1) MANE Select	NP_937884.2:p.Asn1137=
NM_198242.3:c.2919T= (EIF4G1)	NP_937885.1:p.Asn973=
NM_198244.3:c.3150T= (EIF4G1)	NP_937887.2:p.Asn1050=
NM_001194947.2:c.3432T= (EIF4G1)	NP_001181876.2:p.Asn1144=