Canonical Allele Identifier: CA403957629
Gene: EIF3G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115487C>G , CM000681.2:g.10115487C>G GRCh38
NC_000019.9:g.10226163C>G , CM000681.1:g.10226163C>G GRCh37
NC_000019.8:g.10087163C>G NCBI36
NG_047007.1:g.8967C>G
NG_051197.1:g.9438G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.939G>C MANE Select ENSP00000253108.3:p.Glu313Asp
ENST00000253108.8:c.939G>C ENSP00000253108.3:p.Glu313Asp
ENST00000590158.1:n.958G>C
ENST00000593054.5:c.333G>C ENSP00000467187.1:p.Glu111Asp
NM_003755.3:c.939G>C NP_003746.2:p.Glu313Asp
NM_003755.4:c.939G>C NP_003746.2:p.Glu313Asp
NM_003755.5:c.939G>C MANE Select NP_003746.2:p.Glu313Asp