Canonical Allele Identifier: CA2668839725

Gene: EIF4G1 EIF2B5

Linked Data

• gnomAD v4: 3-184327008-T-TAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184327009_184327010insACA , CM000665.2:g.184327009_184327010insACA	GRCh38
NC_000003.11:g.184044797_184044798insACA , CM000665.1:g.184044797_184044798insACA	GRCh37
NC_000003.10:g.185527491_185527492insACA	NCBI36
NG_016850.1:g.17442_17443insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346169.7:c.3428+26_3428+27insACA (EIF4G1) MANE Select	ENSP00000316879.5:n.3428+26_3428+27insACA
ENST00000435046.7:c.3362+26_3362+27insACA (EIF4G1)	ENSP00000404754.3:n.3362+26_3362+27insACA
ENST00000676453.1:c.2775+26_2775+27insACA (EIF4G1)	ENSP00000501695.1:n.2775+26_2775+27insACA
ENST00000319274.10:c.2834+26_2834+27insACA (EIF4G1)	ENSP00000323737.7:n.2834+26_2834+27insACA
ENST00000342981.8:c.3431+26_3431+27insACA (EIF4G1)	ENSP00000343450.4:n.3431+26_3431+27insACA
ENST00000346169.6:c.3428+26_3428+27insACA (EIF4G1)	ENSP00000316879.4:n.3428+26_3428+27insACA
ENST00000350481.9:c.2936+26_2936+27insACA (EIF4G1)	ENSP00000317600.8:n.2936+26_2936+27insACA
ENST00000352767.7:c.3449+26_3449+27insACA (EIF4G1)	ENSP00000338020.4:n.3449+26_3449+27insACA
ENST00000382330.7:c.3449+26_3449+27insACA (EIF4G1)	ENSP00000371767.3:n.3449+26_3449+27insACA
ENST00000392537.6:c.3167+26_3167+27insACA (EIF4G1)	ENSP00000376320.2:n.3167+26_3167+27insACA
ENST00000411531.5:c.3311+26_3311+27insACA (EIF4G1)	ENSP00000395974.1:n.3311+26_3311+27insACA
ENST00000414031.5:c.3308+26_3308+27insACA (EIF4G1)	ENSP00000391935.1:n.3308+26_3308+27insACA
ENST00000424196.5:c.3449+26_3449+27insACA (EIF4G1)	ENSP00000416255.1:n.3449+26_3449+27insACA
ENST00000427845.5:c.3170+26_3170+27insACA (EIF4G1)	ENSP00000407682.1:n.3170+26_3170+27insACA
ENST00000434061.6:c.2843+26_2843+27insACA (EIF4G1)	ENSP00000411826.2:n.2843+26_2843+27insACA
ENST00000435046.6:c.2840+26_2840+27insACA (EIF4G1)	ENSP00000404754.2:n.2840+26_2840+27insACA
ENST00000441154.5:c.2939+26_2939+27insACA (EIF4G1)	ENSP00000399858.1:n.2939+26_2939+27insACA
ENST00000442406.5:c.*2867+26_*2867+27insACA (EIF4G1)	ENSP00000400351.1:n.*2867+26_*2867+27insACA
ENST00000444495.1:c.2106+182302_2106+182303insACA (EIF2B5)	ENSP00000409142.1:n.2106+182302_2106+182303insACA
ENST00000448284.1:c.589+26_589+27insACA (EIF4G1)
NM_001194946.1:c.3449+26_3449+27insACA (EIF4G1)	NP_001181875.1:n.3449+26_3449+27insACA
NM_001194947.1:c.3449+26_3449+27insACA (EIF4G1)	NP_001181876.1:n.3449+26_3449+27insACA
NM_001291157.1:c.3308+26_3308+27insACA (EIF4G1)	NP_001278086.1:n.3308+26_3308+27insACA
NM_004953.4:c.2843+26_2843+27insACA (EIF4G1)	NP_004944.3:n.2843+26_2843+27insACA
NM_182917.4:c.3431+26_3431+27insACA (EIF4G1)	NP_886553.3:n.3431+26_3431+27insACA
NM_198241.2:c.3428+26_3428+27insACA (EIF4G1)	NP_937884.1:n.3428+26_3428+27insACA
NM_198242.2:c.2936+26_2936+27insACA (EIF4G1)	NP_937885.1:n.2936+26_2936+27insACA
NM_198244.2:c.3167+26_3167+27insACA (EIF4G1)	NP_937887.1:n.3167+26_3167+27insACA
NM_001194946.2:c.3449+26_3449+27insACA (EIF4G1)	NP_001181875.2:n.3449+26_3449+27insACA
NM_001291157.2:c.3308+26_3308+27insACA (EIF4G1)	NP_001278086.2:n.3308+26_3308+27insACA
NM_004953.5:c.2843+26_2843+27insACA (EIF4G1)	NP_004944.3:n.2843+26_2843+27insACA
NM_198241.3:c.3428+26_3428+27insACA (EIF4G1) MANE Select	NP_937884.2:n.3428+26_3428+27insACA
NM_198242.3:c.2936+26_2936+27insACA (EIF4G1)	NP_937885.1:n.2936+26_2936+27insACA
NM_198244.3:c.3167+26_3167+27insACA (EIF4G1)	NP_937887.2:n.3167+26_3167+27insACA
NM_001194947.2:c.3449+26_3449+27insACA (EIF4G1)	NP_001181876.2:n.3449+26_3449+27insACA