Canonical Allele Identifier: CA2732896

Gene: EIF4G1 EIF2B5

Linked Data

• dbSNP Id: rs745917508
• ExAC: 3:184045406 C / G
• gnomAD v2: 3-184045406-C-G
• gnomAD v4: 3-184327618-C-G
• MyVariant Identifiers: chr3:g.184045406C>G (hg19) ; chr3:g.184327618C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184327618C>G , CM000665.2:g.184327618C>G	GRCh38
NC_000003.11:g.184045406C>G , CM000665.1:g.184045406C>G	GRCh37
NC_000003.10:g.185528100C>G	NCBI36
NG_016850.1:g.18051C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3694C>G (EIF4G1) MANE Select	ENSP00000316879.5:p.Pro1232Ala
ENST00000435046.7:c.3628C>G (EIF4G1)	ENSP00000404754.3:p.Pro1210Ala
ENST00000676453.1:c.3041C>G (EIF4G1)	ENSP00000501695.1:n.3041C>G
ENST00000319274.10:c.3097C>G (EIF4G1)	ENSP00000323737.7:p.Pro1033Ala
ENST00000342981.8:c.3697C>G (EIF4G1)	ENSP00000343450.4:p.Pro1233Ala
ENST00000346169.6:c.3694C>G (EIF4G1)	ENSP00000316879.4:p.Pro1232Ala
ENST00000350481.9:c.3202C>G (EIF4G1)	ENSP00000317600.8:p.Pro1068Ala
ENST00000352767.7:c.3715C>G (EIF4G1)	ENSP00000338020.4:p.Pro1239Ala
ENST00000382330.7:c.3715C>G (EIF4G1)	ENSP00000371767.3:p.Pro1239Ala
ENST00000392537.6:c.3433C>G (EIF4G1)	ENSP00000376320.2:p.Pro1145Ala
ENST00000411531.5:c.3577C>G (EIF4G1)	ENSP00000395974.1:p.Pro1193Ala
ENST00000414031.5:c.3574C>G (EIF4G1)	ENSP00000391935.1:p.Pro1192Ala
ENST00000424196.5:c.3715C>G (EIF4G1)	ENSP00000416255.1:p.Pro1239Ala
ENST00000427845.5:c.3436C>G (EIF4G1)	ENSP00000407682.1:p.Pro1146Ala
ENST00000434061.6:c.3109C>G (EIF4G1)	ENSP00000411826.2:p.Pro1037Ala
ENST00000435046.6:c.3106C>G (EIF4G1)	ENSP00000404754.2:p.Pro1036Ala
ENST00000441154.5:c.3205C>G (EIF4G1)	ENSP00000399858.1:p.Pro1069Ala
ENST00000442406.5:c.*3133C>G (EIF4G1)	ENSP00000400351.1:n.*3133C>G
ENST00000444495.1:c.2106+182911C>G (EIF2B5)	ENSP00000409142.1:n.2106+182911C>G
ENST00000482303.1:n.196C>G (EIF4G1)
NM_001194946.1:c.3715C>G (EIF4G1)	NP_001181875.1:p.Pro1239Ala
NM_001194947.1:c.3715C>G (EIF4G1)	NP_001181876.1:p.Pro1239Ala
NM_001291157.1:c.3574C>G (EIF4G1)	NP_001278086.1:p.Pro1192Ala
NM_004953.4:c.3109C>G (EIF4G1)	NP_004944.3:p.Pro1037Ala
NM_182917.4:c.3697C>G (EIF4G1)	NP_886553.3:p.Pro1233Ala
NM_198241.2:c.3694C>G (EIF4G1)	NP_937884.1:p.Pro1232Ala
NM_198242.2:c.3202C>G (EIF4G1)	NP_937885.1:p.Pro1068Ala
NM_198244.2:c.3433C>G (EIF4G1)	NP_937887.1:p.Pro1145Ala
NM_001194946.2:c.3715C>G (EIF4G1)	NP_001181875.2:p.Pro1239Ala
NM_001291157.2:c.3574C>G (EIF4G1)	NP_001278086.2:p.Pro1192Ala
NM_004953.5:c.3109C>G (EIF4G1)	NP_004944.3:p.Pro1037Ala
NM_198241.3:c.3694C>G (EIF4G1) MANE Select	NP_937884.2:p.Pro1232Ala
NM_198242.3:c.3202C>G (EIF4G1)	NP_937885.1:p.Pro1068Ala
NM_198244.3:c.3433C>G (EIF4G1)	NP_937887.2:p.Pro1145Ala
NM_001194947.2:c.3715C>G (EIF4G1)	NP_001181876.2:p.Pro1239Ala