Canonical Allele Identifier: CA1425976055

Gene: EIF4G1 EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184319745A= , CM000665.2:g.184319745A=	GRCh38
NC_000003.11:g.184037533A= , CM000665.1:g.184037533A=	GRCh37
NC_000003.10:g.185520227A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.481A= (EIF4G1) MANE Select	ENSP00000316879.5:p.Thr161=
ENST00000435046.7:c.415A= (EIF4G1)	ENSP00000404754.3:p.Thr139=
ENST00000676206.1:c.57A= (EIF4G1)
ENST00000342981.8:c.481A= (EIF4G1)	ENSP00000343450.4:p.Thr161=
ENST00000346169.6:c.481A= (EIF4G1)	ENSP00000316879.4:p.Thr161=
ENST00000350481.9:c.-12A= (EIF4G1)	ENSP00000317600.8:n.-12A=
ENST00000352767.7:c.502A= (EIF4G1)	ENSP00000338020.4:p.Thr168=
ENST00000382330.7:c.502A= (EIF4G1)	ENSP00000371767.3:p.Thr168=
ENST00000392537.6:c.220A= (EIF4G1)	ENSP00000376320.2:p.Thr74=
ENST00000411531.5:c.361A= (EIF4G1)	ENSP00000395974.1:p.Thr121=
ENST00000413967.5:c.204A= (EIF4G1)	ENSP00000390755.1:p.Pro68=
ENST00000414031.5:c.361A= (EIF4G1)	ENSP00000391935.1:p.Thr121=
ENST00000421110.5:c.502A= (EIF4G1)	ENSP00000413159.1:p.Thr168=
ENST00000424196.5:c.502A= (EIF4G1)	ENSP00000416255.1:p.Thr168=
ENST00000426123.5:c.304A= (EIF4G1)	ENSP00000403269.1:p.Thr102=
ENST00000427141.6:c.220A= (EIF4G1)	ENSP00000411214.2:p.Thr74=
ENST00000427845.5:c.220A= (EIF4G1)	ENSP00000407682.1:p.Thr74=
ENST00000442406.5:c.-12A= (EIF4G1)	ENSP00000400351.1:n.-12A=
ENST00000444134.5:c.-51-885A= (EIF4G1)	ENSP00000407244.1:n.-51-885A=
ENST00000444495.1:c.2106+175038A= (EIF2B5)	ENSP00000409142.1:n.2106+175038A=
ENST00000444861.5:c.-12A= (EIF4G1)	ENSP00000398145.1:n.-12A=
ENST00000450424.5:c.481A= (EIF4G1)	ENSP00000391412.1:p.Thr161=
ENST00000456033.5:c.331A= (EIF4G1)	ENSP00000415943.1:p.Thr111=
ENST00000484862.5:n.121A= (EIF4G1)
NM_001194946.2:c.502A= (EIF4G1)	NP_001181875.2:p.Thr168=
NM_001291157.2:c.361A= (EIF4G1)	NP_001278086.2:p.Thr121=
NM_198241.3:c.481A= (EIF4G1) MANE Select	NP_937884.2:p.Thr161=
NM_198242.3:c.-12A= (EIF4G1)	NP_937885.1:n.-12A=
NM_198244.3:c.220A= (EIF4G1)	NP_937887.2:p.Thr74=
NM_001194947.2:c.502A= (EIF4G1)	NP_001181876.2:p.Thr168=