Canonical Allele Identifier: CA505466944

Gene: EIF3G

Linked Data

• MyVariant Identifiers: chr19:g.10226235G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115559G>T , CM000681.2:g.10115559G>T	GRCh38
NC_000019.9:g.10226235G>T , CM000681.1:g.10226235G>T	GRCh37
NC_000019.8:g.10087235G>T	NCBI36
NG_047007.1:g.9039G>T
NG_051197.1:g.9366C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253108.9:c.867C>A MANE Select	ENSP00000253108.3:p.Arg289=
ENST00000253108.8:c.867C>A	ENSP00000253108.3:p.Arg289=
ENST00000589454.5:c.843C>A	ENSP00000466860.1:p.Arg281=
ENST00000590158.1:n.886C>A
ENST00000593054.5:c.261C>A	ENSP00000467187.1:p.Arg87=
NM_003755.3:c.867C>A	NP_003746.2:p.Arg289=
NM_003755.4:c.867C>A	NP_003746.2:p.Arg289=
NM_003755.5:c.867C>A MANE Select	NP_003746.2:p.Arg289=