Canonical Allele Identifier: CA403957825
Gene: EIF3G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115537T>C , CM000681.2:g.10115537T>C GRCh38
NC_000019.9:g.10226213T>C , CM000681.1:g.10226213T>C GRCh37
NC_000019.8:g.10087213T>C NCBI36
NG_047007.1:g.9017T>C
NG_051197.1:g.9388A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.889A>G MANE Select ENSP00000253108.3:p.Ile297Val
ENST00000253108.8:c.889A>G ENSP00000253108.3:p.Ile297Val
ENST00000589454.5:c.865A>G ENSP00000466860.1:p.Ile289Val
ENST00000590158.1:n.908A>G
ENST00000593054.5:c.283A>G ENSP00000467187.1:p.Ile95Val
NM_003755.3:c.889A>G NP_003746.2:p.Ile297Val
NM_003755.4:c.889A>G NP_003746.2:p.Ile297Val
NM_003755.5:c.889A>G MANE Select NP_003746.2:p.Ile297Val