Canonical Allele Identifier: CA505466896

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226214G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115538G>T , CM000681.2:g.10115538G>T	GRCh38
NC_000019.9:g.10226214G>T , CM000681.1:g.10226214G>T	GRCh37
NC_000019.8:g.10087214G>T	NCBI36
NG_047007.1:g.9018G>T
NG_051197.1:g.9387C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.888C>A MANE Select	ENSP00000253108.3:p.Ala296=
ENST00000253108.8:c.888C>A	ENSP00000253108.3:p.Ala296=
ENST00000589454.5:c.864C>A	ENSP00000466860.1:p.Ala288=
ENST00000590158.1:n.907C>A
ENST00000593054.5:c.282C>A	ENSP00000467187.1:p.Ala94=
NM_003755.3:c.888C>A	NP_003746.2:p.Ala296=
NM_003755.4:c.888C>A	NP_003746.2:p.Ala296=
NM_003755.5:c.888C>A MANE Select	NP_003746.2:p.Ala296=