Canonical Allele Identifier: CA2322270392
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115653A= , CM000681.2:g.10115653A= GRCh38
NC_000019.9:g.10226329A= , CM000681.1:g.10226329A= GRCh37
NC_000019.8:g.10087329A= NCBI36
NG_047007.1:g.9133A=
NG_051197.1:g.9272T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+31T= MANE Select ENSP00000253108.3:n.840+31T=
ENST00000253108.8:c.840+31T= ENSP00000253108.3:n.840+31T=
ENST00000589454.5:c.816+31T= ENSP00000466860.1:n.816+31T=
ENST00000590158.1:n.859+31T=
ENST00000593054.5:c.234+31T= ENSP00000467187.1:n.234+31T=
NM_003755.3:c.840+31T= NP_003746.2:n.840+31T=
NM_003755.4:c.840+31T= NP_003746.2:n.840+31T=
NM_003755.5:c.840+31T= MANE Select NP_003746.2:n.840+31T=