Canonical Allele Identifier: CA2322270338
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115572A= , CM000681.2:g.10115572A= GRCh38
NC_000019.9:g.10226248A= , CM000681.1:g.10226248A= GRCh37
NC_000019.8:g.10087248A= NCBI36
NG_047007.1:g.9052A=
NG_051197.1:g.9353T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.854T= MANE Select ENSP00000253108.3:p.Ile285=
ENST00000253108.8:c.854T= ENSP00000253108.3:p.Ile285=
ENST00000589454.5:c.830T= ENSP00000466860.1:p.Ile277=
ENST00000590158.1:n.873T=
ENST00000593054.5:c.248T= ENSP00000467187.1:p.Ile83=
NM_003755.3:c.854T= NP_003746.2:p.Ile285=
NM_003755.4:c.854T= NP_003746.2:p.Ile285=
NM_003755.5:c.854T= MANE Select NP_003746.2:p.Ile285=