Canonical Allele Identifier: CA403957851
Gene: EIF3G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115548G>C , CM000681.2:g.10115548G>C GRCh38
NC_000019.9:g.10226224G>C , CM000681.1:g.10226224G>C GRCh37
NC_000019.8:g.10087224G>C NCBI36
NG_047007.1:g.9028G>C
NG_051197.1:g.9377C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.878C>G MANE Select ENSP00000253108.3:p.Ala293Gly
ENST00000253108.8:c.878C>G ENSP00000253108.3:p.Ala293Gly
ENST00000589454.5:c.854C>G ENSP00000466860.1:p.Ala285Gly
ENST00000590158.1:n.897C>G
ENST00000593054.5:c.272C>G ENSP00000467187.1:p.Ala91Gly
NM_003755.3:c.878C>G NP_003746.2:p.Ala293Gly
NM_003755.4:c.878C>G NP_003746.2:p.Ala293Gly
NM_003755.5:c.878C>G MANE Select NP_003746.2:p.Ala293Gly