Canonical Allele Identifier: CA2322270391
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115651A= , CM000681.2:g.10115651A= GRCh38
NC_000019.9:g.10226327A= , CM000681.1:g.10226327A= GRCh37
NC_000019.8:g.10087327A= NCBI36
NG_047007.1:g.9131A=
NG_051197.1:g.9274T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+33T= MANE Select ENSP00000253108.3:n.840+33T=
ENST00000253108.8:c.840+33T= ENSP00000253108.3:n.840+33T=
ENST00000589454.5:c.816+33T= ENSP00000466860.1:n.816+33T=
ENST00000590158.1:n.859+33T=
ENST00000593054.5:c.234+33T= ENSP00000467187.1:n.234+33T=
NM_003755.3:c.840+33T= NP_003746.2:n.840+33T=
NM_003755.4:c.840+33T= NP_003746.2:n.840+33T=
NM_003755.5:c.840+33T= MANE Select NP_003746.2:n.840+33T=