Canonical Allele Identifier: CA2813565541
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115651A>G , CM000681.2:g.10115651A>G GRCh38
NC_000019.9:g.10226327A>G , CM000681.1:g.10226327A>G GRCh37
NC_000019.8:g.10087327A>G NCBI36
NG_047007.1:g.9131A>G
NG_051197.1:g.9274T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+33T>C MANE Select ENSP00000253108.3:n.840+33T>C
ENST00000253108.8:c.840+33T>C ENSP00000253108.3:n.840+33T>C
ENST00000589454.5:c.816+33T>C ENSP00000466860.1:n.816+33T>C
ENST00000590158.1:n.859+33T>C
ENST00000593054.5:c.234+33T>C ENSP00000467187.1:n.234+33T>C
NM_003755.3:c.840+33T>C NP_003746.2:n.840+33T>C
NM_003755.4:c.840+33T>C NP_003746.2:n.840+33T>C
NM_003755.5:c.840+33T>C MANE Select NP_003746.2:n.840+33T>C