Canonical Allele Identifier: CA2517913167
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115637_10115638insC , CM000681.2:g.10115637_10115638insC GRCh38
NC_000019.9:g.10226313_10226314insC , CM000681.1:g.10226313_10226314insC GRCh37
NC_000019.8:g.10087313_10087314insC NCBI36
NG_047007.1:g.9117_9118insC
NG_051197.1:g.9287_9288insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+46_840+47insG MANE Select ENSP00000253108.3:n.840+46_840+47insG
ENST00000253108.8:c.840+46_840+47insG ENSP00000253108.3:n.840+46_840+47insG
ENST00000589454.5:c.816+46_816+47insG ENSP00000466860.1:n.816+46_816+47insG
ENST00000590158.1:n.859+46_859+47insG
ENST00000593054.5:c.234+46_234+47insG ENSP00000467187.1:n.234+46_234+47insG
NM_003755.3:c.840+46_840+47insG NP_003746.2:n.840+46_840+47insG
NM_003755.4:c.840+46_840+47insG NP_003746.2:n.840+46_840+47insG
NM_003755.5:c.840+46_840+47insG MANE Select NP_003746.2:n.840+46_840+47insG