Canonical Allele Identifier: CA403957732

Gene: EIF3G

Linked Data

• COSMIC: COSM6298315
• MyVariant Identifiers: chr19:g.10226187G>T (hg19) ; chr19:g.10115511G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115511G>T , CM000681.2:g.10115511G>T	GRCh38
NC_000019.9:g.10226187G>T , CM000681.1:g.10226187G>T	GRCh37
NC_000019.8:g.10087187G>T	NCBI36
NG_047007.1:g.8991G>T
NG_051197.1:g.9414C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000253108.9:c.915C>A MANE Select	ENSP00000253108.3:p.Tyr305Ter
ENST00000253108.8:c.915C>A	ENSP00000253108.3:p.Tyr305Ter
ENST00000590158.1:n.934C>A
ENST00000593054.5:c.309C>A	ENSP00000467187.1:p.Tyr103Ter
NM_003755.3:c.915C>A	NP_003746.2:p.Tyr305Ter
NM_003755.4:c.915C>A	NP_003746.2:p.Tyr305Ter
NM_003755.5:c.915C>A MANE Select	NP_003746.2:p.Tyr305Ter