Canonical Allele Identifier: CA403957998

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226257A>C (hg19) ; chr19:g.10115581A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115581A>C , CM000681.2:g.10115581A>C	GRCh38
NC_000019.9:g.10226257A>C , CM000681.1:g.10226257A>C	GRCh37
NC_000019.8:g.10087257A>C	NCBI36
NG_047007.1:g.9061A>C
NG_051197.1:g.9344T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.845T>G MANE Select	ENSP00000253108.3:p.Phe282Cys
ENST00000253108.8:c.845T>G	ENSP00000253108.3:p.Phe282Cys
ENST00000589454.5:c.821T>G	ENSP00000466860.1:p.Phe274Cys
ENST00000590158.1:n.864T>G
ENST00000593054.5:c.239T>G	ENSP00000467187.1:p.Phe80Cys
NM_003755.3:c.845T>G	NP_003746.2:p.Phe282Cys
NM_003755.4:c.845T>G	NP_003746.2:p.Phe282Cys
NM_003755.5:c.845T>G MANE Select	NP_003746.2:p.Phe282Cys