Canonical Allele Identifier: CA403957885

Gene: EIF3G

Linked Data

• gnomAD v4: 19-10115555-C-T
• COSMIC: COSM5745379
• MyVariant Identifiers: chr19:g.10226231C>T (hg19) ; chr19:g.10115555C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115555C>T , CM000681.2:g.10115555C>T	GRCh38
NC_000019.9:g.10226231C>T , CM000681.1:g.10226231C>T	GRCh37
NC_000019.8:g.10087231C>T	NCBI36
NG_047007.1:g.9035C>T
NG_051197.1:g.9370G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.871G>A MANE Select	ENSP00000253108.3:p.Glu291Lys
ENST00000253108.8:c.871G>A	ENSP00000253108.3:p.Glu291Lys
ENST00000589454.5:c.847G>A	ENSP00000466860.1:p.Glu283Lys
ENST00000590158.1:n.890G>A
ENST00000593054.5:c.265G>A	ENSP00000467187.1:p.Glu89Lys
NM_003755.3:c.871G>A	NP_003746.2:p.Glu291Lys
NM_003755.4:c.871G>A	NP_003746.2:p.Glu291Lys
NM_003755.5:c.871G>A MANE Select	NP_003746.2:p.Glu291Lys