Canonical Allele Identifier: CA2576615779
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115657C>A , CM000681.2:g.10115657C>A GRCh38
NC_000019.9:g.10226333C>A , CM000681.1:g.10226333C>A GRCh37
NC_000019.8:g.10087333C>A NCBI36
NG_047007.1:g.9137C>A
NG_051197.1:g.9268G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+27G>T MANE Select ENSP00000253108.3:n.840+27G>T
ENST00000253108.8:c.840+27G>T ENSP00000253108.3:n.840+27G>T
ENST00000589454.5:c.816+27G>T ENSP00000466860.1:n.816+27G>T
ENST00000590158.1:n.859+27G>T
ENST00000593054.5:c.234+27G>T ENSP00000467187.1:n.234+27G>T
NM_003755.3:c.840+27G>T NP_003746.2:n.840+27G>T
NM_003755.4:c.840+27G>T NP_003746.2:n.840+27G>T
NM_003755.5:c.840+27G>T MANE Select NP_003746.2:n.840+27G>T