Canonical Allele Identifier: CA403957638

Gene: EIF3G

Linked Data

• COSMIC: COSM5706832
• MyVariant Identifiers: chr19:g.10226165C>G (hg19) ; chr19:g.10115489C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115489C>G , CM000681.2:g.10115489C>G	GRCh38
NC_000019.9:g.10226165C>G , CM000681.1:g.10226165C>G	GRCh37
NC_000019.8:g.10087165C>G	NCBI36
NG_047007.1:g.8969C>G
NG_051197.1:g.9436G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.937G>C MANE Select	ENSP00000253108.3:p.Glu313Gln
ENST00000253108.8:c.937G>C	ENSP00000253108.3:p.Glu313Gln
ENST00000590158.1:n.956G>C
ENST00000593054.5:c.331G>C	ENSP00000467187.1:p.Glu111Gln
NM_003755.3:c.937G>C	NP_003746.2:p.Glu313Gln
NM_003755.4:c.937G>C	NP_003746.2:p.Glu313Gln
NM_003755.5:c.937G>C MANE Select	NP_003746.2:p.Glu313Gln