Canonical Allele Identifier: CA505466909

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226220C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115544C>G , CM000681.2:g.10115544C>G	GRCh38
NC_000019.9:g.10226220C>G , CM000681.1:g.10226220C>G	GRCh37
NC_000019.8:g.10087220C>G	NCBI36
NG_047007.1:g.9024C>G
NG_051197.1:g.9381G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.882G>C MANE Select	ENSP00000253108.3:p.Ala294=
ENST00000253108.8:c.882G>C	ENSP00000253108.3:p.Ala294=
ENST00000589454.5:c.858G>C	ENSP00000466860.1:p.Ala286=
ENST00000590158.1:n.901G>C
ENST00000593054.5:c.276G>C	ENSP00000467187.1:p.Ala92=
NM_003755.3:c.882G>C	NP_003746.2:p.Ala294=
NM_003755.4:c.882G>C	NP_003746.2:p.Ala294=
NM_003755.5:c.882G>C MANE Select	NP_003746.2:p.Ala294=