Canonical Allele Identifier: CA437330554

Gene: EIF4G1 EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.184045396C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184327608C>A , CM000665.2:g.184327608C>A	GRCh38
NC_000003.11:g.184045396C>A , CM000665.1:g.184045396C>A	GRCh37
NC_000003.10:g.185528090C>A	NCBI36
NG_016850.1:g.18041C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3684C>A (EIF4G1) MANE Select	ENSP00000316879.5:p.Pro1228=
ENST00000435046.7:c.3618C>A (EIF4G1)	ENSP00000404754.3:p.Pro1206=
ENST00000676453.1:c.3031C>A (EIF4G1)	ENSP00000501695.1:n.3031C>A
ENST00000319274.10:c.3087C>A (EIF4G1)	ENSP00000323737.7:p.Pro1029=
ENST00000342981.8:c.3687C>A (EIF4G1)	ENSP00000343450.4:p.Pro1229=
ENST00000346169.6:c.3684C>A (EIF4G1)	ENSP00000316879.4:p.Pro1228=
ENST00000350481.9:c.3192C>A (EIF4G1)	ENSP00000317600.8:p.Pro1064=
ENST00000352767.7:c.3705C>A (EIF4G1)	ENSP00000338020.4:p.Pro1235=
ENST00000382330.7:c.3705C>A (EIF4G1)	ENSP00000371767.3:p.Pro1235=
ENST00000392537.6:c.3423C>A (EIF4G1)	ENSP00000376320.2:p.Pro1141=
ENST00000411531.5:c.3567C>A (EIF4G1)	ENSP00000395974.1:p.Pro1189=
ENST00000414031.5:c.3564C>A (EIF4G1)	ENSP00000391935.1:p.Pro1188=
ENST00000424196.5:c.3705C>A (EIF4G1)	ENSP00000416255.1:p.Pro1235=
ENST00000427845.5:c.3426C>A (EIF4G1)	ENSP00000407682.1:p.Pro1142=
ENST00000434061.6:c.3099C>A (EIF4G1)	ENSP00000411826.2:p.Pro1033=
ENST00000435046.6:c.3096C>A (EIF4G1)	ENSP00000404754.2:p.Pro1032=
ENST00000441154.5:c.3195C>A (EIF4G1)	ENSP00000399858.1:p.Pro1065=
ENST00000442406.5:c.*3123C>A (EIF4G1)	ENSP00000400351.1:n.*3123C>A
ENST00000444495.1:c.2106+182901C>A (EIF2B5)	ENSP00000409142.1:n.2106+182901C>A
ENST00000482303.1:n.186C>A (EIF4G1)
NM_001194946.1:c.3705C>A (EIF4G1)	NP_001181875.1:p.Pro1235=
NM_001194947.1:c.3705C>A (EIF4G1)	NP_001181876.1:p.Pro1235=
NM_001291157.1:c.3564C>A (EIF4G1)	NP_001278086.1:p.Pro1188=
NM_004953.4:c.3099C>A (EIF4G1)	NP_004944.3:p.Pro1033=
NM_182917.4:c.3687C>A (EIF4G1)	NP_886553.3:p.Pro1229=
NM_198241.2:c.3684C>A (EIF4G1)	NP_937884.1:p.Pro1228=
NM_198242.2:c.3192C>A (EIF4G1)	NP_937885.1:p.Pro1064=
NM_198244.2:c.3423C>A (EIF4G1)	NP_937887.1:p.Pro1141=
NM_001194946.2:c.3705C>A (EIF4G1)	NP_001181875.2:p.Pro1235=
NM_001291157.2:c.3564C>A (EIF4G1)	NP_001278086.2:p.Pro1188=
NM_004953.5:c.3099C>A (EIF4G1)	NP_004944.3:p.Pro1033=
NM_198241.3:c.3684C>A (EIF4G1) MANE Select	NP_937884.2:p.Pro1228=
NM_198242.3:c.3192C>A (EIF4G1)	NP_937885.1:p.Pro1064=
NM_198244.3:c.3423C>A (EIF4G1)	NP_937887.2:p.Pro1141=
NM_001194947.2:c.3705C>A (EIF4G1)	NP_001181876.2:p.Pro1235=