Canonical Allele Identifier: CA403957630

Gene: EIF3G

Linked Data

• gnomAD v4: 19-10115487-C-A
• MyVariant Identifiers: chr19:g.10226163C>A (hg19) ; chr19:g.10115487C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115487C>A , CM000681.2:g.10115487C>A	GRCh38
NC_000019.9:g.10226163C>A , CM000681.1:g.10226163C>A	GRCh37
NC_000019.8:g.10087163C>A	NCBI36
NG_047007.1:g.8967C>A
NG_051197.1:g.9438G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000253108.9:c.939G>T MANE Select	ENSP00000253108.3:p.Glu313Asp
ENST00000253108.8:c.939G>T	ENSP00000253108.3:p.Glu313Asp
ENST00000590158.1:n.958G>T
ENST00000593054.5:c.333G>T	ENSP00000467187.1:p.Glu111Asp
NM_003755.3:c.939G>T	NP_003746.2:p.Glu313Asp
NM_003755.4:c.939G>T	NP_003746.2:p.Glu313Asp
NM_003755.5:c.939G>T MANE Select	NP_003746.2:p.Glu313Asp