Canonical Allele Identifier: CA2555628607
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115643_10115644insCAG , CM000681.2:g.10115643_10115644insCAG GRCh38
NC_000019.9:g.10226319_10226320insCAG , CM000681.1:g.10226319_10226320insCAG GRCh37
NC_000019.8:g.10087319_10087320insCAG NCBI36
NG_047007.1:g.9123_9124insCAG
NG_051197.1:g.9281_9282insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.840+40_840+41insCTG MANE Select ENSP00000253108.3:n.840+40_840+41insCTG
ENST00000253108.8:c.840+40_840+41insCTG ENSP00000253108.3:n.840+40_840+41insCTG
ENST00000589454.5:c.816+40_816+41insCTG ENSP00000466860.1:n.816+40_816+41insCTG
ENST00000590158.1:n.859+40_859+41insCTG
ENST00000593054.5:c.234+40_234+41insCTG ENSP00000467187.1:n.234+40_234+41insCTG
NM_003755.3:c.840+40_840+41insCTG NP_003746.2:n.840+40_840+41insCTG
NM_003755.4:c.840+40_840+41insCTG NP_003746.2:n.840+40_840+41insCTG
NM_003755.5:c.840+40_840+41insCTG MANE Select NP_003746.2:n.840+40_840+41insCTG