Canonical Allele Identifier: CA2322270386
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115643T= , CM000681.2:g.10115643T= GRCh38
NC_000019.9:g.10226319T= , CM000681.1:g.10226319T= GRCh37
NC_000019.8:g.10087319T= NCBI36
NG_047007.1:g.9123T=
NG_051197.1:g.9282A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+41A= MANE Select ENSP00000253108.3:n.840+41A=
ENST00000253108.8:c.840+41A= ENSP00000253108.3:n.840+41A=
ENST00000589454.5:c.816+41A= ENSP00000466860.1:n.816+41A=
ENST00000590158.1:n.859+41A=
ENST00000593054.5:c.234+41A= ENSP00000467187.1:n.234+41A=
NM_003755.3:c.840+41A= NP_003746.2:n.840+41A=
NM_003755.4:c.840+41A= NP_003746.2:n.840+41A=
NM_003755.5:c.840+41A= MANE Select NP_003746.2:n.840+41A=