Canonical Allele Identifier: CA403957988
Gene: EIF3G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115579C>G , CM000681.2:g.10115579C>G GRCh38
NC_000019.9:g.10226255C>G , CM000681.1:g.10226255C>G GRCh37
NC_000019.8:g.10087255C>G NCBI36
NG_047007.1:g.9059C>G
NG_051197.1:g.9346G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.847G>C MANE Select ENSP00000253108.3:p.Ala283Pro
ENST00000253108.8:c.847G>C ENSP00000253108.3:p.Ala283Pro
ENST00000589454.5:c.823G>C ENSP00000466860.1:p.Ala275Pro
ENST00000590158.1:n.866G>C
ENST00000593054.5:c.241G>C ENSP00000467187.1:p.Ala81Pro
NM_003755.3:c.847G>C NP_003746.2:p.Ala283Pro
NM_003755.4:c.847G>C NP_003746.2:p.Ala283Pro
NM_003755.5:c.847G>C MANE Select NP_003746.2:p.Ala283Pro