Canonical Allele Identifier: CA355413129

Gene: EIF4G1 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184044696G>C (hg19) ; chr3:g.184326908G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184326908G>C , CM000665.2:g.184326908G>C	GRCh38
NC_000003.11:g.184044696G>C , CM000665.1:g.184044696G>C	GRCh37
NC_000003.10:g.185527390G>C	NCBI36
NG_016850.1:g.17341G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3353G>C (EIF4G1) MANE Select	ENSP00000316879.5:p.Ser1118Thr
ENST00000435046.7:c.3287G>C (EIF4G1)	ENSP00000404754.3:p.Ser1096Thr
ENST00000676453.1:c.2700G>C (EIF4G1)	ENSP00000501695.1:n.2700G>C
ENST00000319274.10:c.2759G>C (EIF4G1)	ENSP00000323737.7:p.Ser920Thr
ENST00000342981.8:c.3356G>C (EIF4G1)	ENSP00000343450.4:p.Ser1119Thr
ENST00000346169.6:c.3353G>C (EIF4G1)	ENSP00000316879.4:p.Ser1118Thr
ENST00000350481.9:c.2861G>C (EIF4G1)	ENSP00000317600.8:p.Ser954Thr
ENST00000352767.7:c.3374G>C (EIF4G1)	ENSP00000338020.4:p.Ser1125Thr
ENST00000382330.7:c.3374G>C (EIF4G1)	ENSP00000371767.3:p.Ser1125Thr
ENST00000392537.6:c.3092G>C (EIF4G1)	ENSP00000376320.2:p.Ser1031Thr
ENST00000411531.5:c.3236G>C (EIF4G1)	ENSP00000395974.1:p.Ser1079Thr
ENST00000414031.5:c.3233G>C (EIF4G1)	ENSP00000391935.1:p.Ser1078Thr
ENST00000424196.5:c.3374G>C (EIF4G1)	ENSP00000416255.1:p.Ser1125Thr
ENST00000427845.5:c.3095G>C (EIF4G1)	ENSP00000407682.1:p.Ser1032Thr
ENST00000434061.6:c.2768G>C (EIF4G1)	ENSP00000411826.2:p.Ser923Thr
ENST00000435046.6:c.2765G>C (EIF4G1)	ENSP00000404754.2:p.Ser922Thr
ENST00000441154.5:c.2864G>C (EIF4G1)	ENSP00000399858.1:p.Ser955Thr
ENST00000442406.5:c.*2792G>C (EIF4G1)	ENSP00000400351.1:n.*2792G>C
ENST00000444495.1:c.2106+182201G>C (EIF2B5)	ENSP00000409142.1:n.2106+182201G>C
ENST00000448284.1:c.514G>C (EIF4G1)
ENST00000466311.1:n.573G>C (EIF4G1)
NM_001194946.1:c.3374G>C (EIF4G1)	NP_001181875.1:p.Ser1125Thr
NM_001194947.1:c.3374G>C (EIF4G1)	NP_001181876.1:p.Ser1125Thr
NM_001291157.1:c.3233G>C (EIF4G1)	NP_001278086.1:p.Ser1078Thr
NM_004953.4:c.2768G>C (EIF4G1)	NP_004944.3:p.Ser923Thr
NM_182917.4:c.3356G>C (EIF4G1)	NP_886553.3:p.Ser1119Thr
NM_198241.2:c.3353G>C (EIF4G1)	NP_937884.1:p.Ser1118Thr
NM_198242.2:c.2861G>C (EIF4G1)	NP_937885.1:p.Ser954Thr
NM_198244.2:c.3092G>C (EIF4G1)	NP_937887.1:p.Ser1031Thr
NM_001194946.2:c.3374G>C (EIF4G1)	NP_001181875.2:p.Ser1125Thr
NM_001291157.2:c.3233G>C (EIF4G1)	NP_001278086.2:p.Ser1078Thr
NM_004953.5:c.2768G>C (EIF4G1)	NP_004944.3:p.Ser923Thr
NM_198241.3:c.3353G>C (EIF4G1) MANE Select	NP_937884.2:p.Ser1118Thr
NM_198242.3:c.2861G>C (EIF4G1)	NP_937885.1:p.Ser954Thr
NM_198244.3:c.3092G>C (EIF4G1)	NP_937887.2:p.Ser1031Thr
NM_001194947.2:c.3374G>C (EIF4G1)	NP_001181876.2:p.Ser1125Thr