Canonical Allele Identifier: CA2322270838
Community Standard Title: NM_003755.5(EIF3G):c.596-260T=
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10116334A= , CM000681.2:g.10116334A= GRCh38
NC_000019.9:g.10227010A= , CM000681.1:g.10227010A= GRCh37
NC_000019.8:g.10088010A= NCBI36
NG_047007.1:g.9814A=
NG_051197.1:g.8591T=

Transcript Alleles

HGVS Amino-acid Change
NM_003755.5:c.596-260T= MANE Select NP_003746.2:n.596-260T=
ENST00000253108.9:c.596-260T= MANE Select ENSP00000253108.3:n.596-260T=
NM_003755.3:c.596-260T= NP_003746.2:n.596-260T=
NM_003755.4:c.596-260T= NP_003746.2:n.596-260T=
ENST00000253108.8:c.596-260T= ENSP00000253108.3:n.596-260T=
ENST00000587146.5:c.491-260T= ENSP00000468159.1:n.491-260T=
ENST00000588709.5:c.602-260T= ENSP00000465882.1:n.602-260T=
ENST00000589009.5:n.1238T=
ENST00000589454.5:c.572-260T= ENSP00000466860.1:n.572-260T=
ENST00000590158.1:n.355T=
ENST00000593054.5:c.29-260T= ENSP00000467187.1:n.29-260T=