Canonical Allele Identifier: CA2322270393
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115654_10115656delinsCAG , CM000681.2:g.10115654_10115656delinsCAG GRCh38
NC_000019.9:g.10226330_10226332delinsCAG , CM000681.1:g.10226330_10226332delinsCAG GRCh37
NC_000019.8:g.10087330_10087332delinsCAG NCBI36
NG_047007.1:g.9134_9136delinsCAG
NG_051197.1:g.9269_9271delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+28_840+30delinsCTG MANE Select ENSP00000253108.3:n.840+28_840+30delinsCTG
ENST00000253108.8:c.840+28_840+30delinsCTG ENSP00000253108.3:n.840+28_840+30delinsCTG
ENST00000589454.5:c.816+28_816+30delinsCTG ENSP00000466860.1:n.816+28_816+30delinsCTG
ENST00000590158.1:n.859+28_859+30delinsCTG
ENST00000593054.5:c.234+28_234+30delinsCTG ENSP00000467187.1:n.234+28_234+30delinsCTG
NM_003755.3:c.840+28_840+30delinsCTG NP_003746.2:n.840+28_840+30delinsCTG
NM_003755.4:c.840+28_840+30delinsCTG NP_003746.2:n.840+28_840+30delinsCTG
NM_003755.5:c.840+28_840+30delinsCTG MANE Select NP_003746.2:n.840+28_840+30delinsCTG