Canonical Allele Identifier: CA403957832
Gene: EIF3G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115540C>T , CM000681.2:g.10115540C>T GRCh38
NC_000019.9:g.10226216C>T , CM000681.1:g.10226216C>T GRCh37
NC_000019.8:g.10087216C>T NCBI36
NG_047007.1:g.9020C>T
NG_051197.1:g.9385G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.886G>A MANE Select ENSP00000253108.3:p.Ala296Thr
ENST00000253108.8:c.886G>A ENSP00000253108.3:p.Ala296Thr
ENST00000589454.5:c.862G>A ENSP00000466860.1:p.Ala288Thr
ENST00000590158.1:n.905G>A
ENST00000593054.5:c.280G>A ENSP00000467187.1:p.Ala94Thr
NM_003755.3:c.886G>A NP_003746.2:p.Ala296Thr
NM_003755.4:c.886G>A NP_003746.2:p.Ala296Thr
NM_003755.5:c.886G>A MANE Select NP_003746.2:p.Ala296Thr