Canonical Allele Identifier: CA2322270397
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115659C= , CM000681.2:g.10115659C= GRCh38
NC_000019.9:g.10226335C= , CM000681.1:g.10226335C= GRCh37
NC_000019.8:g.10087335C= NCBI36
NG_047007.1:g.9139C=
NG_051197.1:g.9266G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+25G= MANE Select ENSP00000253108.3:n.840+25G=
ENST00000253108.8:c.840+25G= ENSP00000253108.3:n.840+25G=
ENST00000589454.5:c.816+25G= ENSP00000466860.1:n.816+25G=
ENST00000590158.1:n.859+25G=
ENST00000593054.5:c.234+25G= ENSP00000467187.1:n.234+25G=
NM_003755.3:c.840+25G= NP_003746.2:n.840+25G=
NM_003755.4:c.840+25G= NP_003746.2:n.840+25G=
NM_003755.5:c.840+25G= MANE Select NP_003746.2:n.840+25G=