Canonical Allele Identifier: CA1425958223
Gene: EIF4G1 HGNC NCBI
EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184327286G= , CM000665.2:g.184327286G= GRCh38
NC_000003.11:g.184045074G= , CM000665.1:g.184045074G= GRCh37
NC_000003.10:g.185527768G= NCBI36
NG_016850.1:g.17719G=

Transcript Alleles

HGVS Amino-acid change
ENST00000346169.7:c.3499G= (EIF4G1) MANE Select ENSP00000316879.5:p.Gly1167=
ENST00000435046.7:c.3433G= (EIF4G1) ENSP00000404754.3:p.Gly1145=
ENST00000676453.1:c.2846G= (EIF4G1) ENSP00000501695.1:n.2846G=
ENST00000319274.10:c.2904G= (EIF4G1) ENSP00000323737.7:p.Gly968=
ENST00000342981.8:c.3502G= (EIF4G1) ENSP00000343450.4:p.Gly1168=
ENST00000346169.6:c.3499G= (EIF4G1) ENSP00000316879.4:p.Gly1167=
ENST00000350481.9:c.3007G= (EIF4G1) ENSP00000317600.8:p.Gly1003=
ENST00000352767.7:c.3520G= (EIF4G1) ENSP00000338020.4:p.Gly1174=
ENST00000382330.7:c.3520G= (EIF4G1) ENSP00000371767.3:p.Gly1174=
ENST00000392537.6:c.3238G= (EIF4G1) ENSP00000376320.2:p.Gly1080=
ENST00000411531.5:c.3382G= (EIF4G1) ENSP00000395974.1:p.Gly1128=
ENST00000414031.5:c.3379G= (EIF4G1) ENSP00000391935.1:p.Gly1127=
ENST00000424196.5:c.3520G= (EIF4G1) ENSP00000416255.1:p.Gly1174=
ENST00000427845.5:c.3241G= (EIF4G1) ENSP00000407682.1:p.Gly1081=
ENST00000434061.6:c.2914G= (EIF4G1) ENSP00000411826.2:p.Gly972=
ENST00000435046.6:c.2911G= (EIF4G1) ENSP00000404754.2:p.Gly971=
ENST00000441154.5:c.3010G= (EIF4G1) ENSP00000399858.1:p.Gly1004=
ENST00000442406.5:c.*2938G= (EIF4G1) ENSP00000400351.1:n.*2938G=
ENST00000444495.1:c.2106+182579G= (EIF2B5) ENSP00000409142.1:n.2106+182579G=
ENST00000448284.1:c.660G= (EIF4G1)
ENST00000482303.1:n.1G= (EIF4G1)
NM_001194946.1:c.3520G= (EIF4G1) NP_001181875.1:p.Gly1174=
NM_001194947.1:c.3520G= (EIF4G1) NP_001181876.1:p.Gly1174=
NM_001291157.1:c.3379G= (EIF4G1) NP_001278086.1:p.Gly1127=
NM_004953.4:c.2914G= (EIF4G1) NP_004944.3:p.Gly972=
NM_182917.4:c.3502G= (EIF4G1) NP_886553.3:p.Gly1168=
NM_198241.2:c.3499G= (EIF4G1) NP_937884.1:p.Gly1167=
NM_198242.2:c.3007G= (EIF4G1) NP_937885.1:p.Gly1003=
NM_198244.2:c.3238G= (EIF4G1) NP_937887.1:p.Gly1080=
NM_001194946.2:c.3520G= (EIF4G1) NP_001181875.2:p.Gly1174=
NM_001291157.2:c.3379G= (EIF4G1) NP_001278086.2:p.Gly1127=
NM_004953.5:c.2914G= (EIF4G1) NP_004944.3:p.Gly972=
NM_198241.3:c.3499G= (EIF4G1) MANE Select NP_937884.2:p.Gly1167=
NM_198242.3:c.3007G= (EIF4G1) NP_937885.1:p.Gly1003=
NM_198244.3:c.3238G= (EIF4G1) NP_937887.2:p.Gly1080=
NM_001194947.2:c.3520G= (EIF4G1) NP_001181876.2:p.Gly1174=