Canonical Allele Identifier: CA2695198123
Gene: EIF3G HGNC NCBI

Linked Data

ClinVar Variation Id: 2671899
ClinVar RCV Id: RCV003458926
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115477dup , CM000681.2:g.10115477dup GRCh38
NC_000019.9:g.10226153dup , CM000681.1:g.10226153dup GRCh37
NC_000019.8:g.10087153dup NCBI36
NG_047007.1:g.8957dup
NG_051197.1:g.9448dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.947+2dup MANE Select ENSP00000253108.3:n.947+2dup
ENST00000253108.8:c.947+2dup ENSP00000253108.3:n.947+2dup
ENST00000590158.1:n.966+2dup
ENST00000593054.5:c.341+2dup ENSP00000467187.1:n.341+2dup
NM_003755.3:c.947+2dup NP_003746.2:n.947+2dup
NM_003755.4:c.947+2dup NP_003746.2:n.947+2dup
NM_003755.5:c.947+2dup MANE Select NP_003746.2:n.947+2dup
Search 100 bp 5'
Search 100 bp 3'