Canonical Allele Identifier: CA2735551567
Gene: EIF3G HGNC NCBI

Linked Data

dbSNP Id: rs2145225833

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115592_10115604del , CM000681.2:g.10115592_10115604del GRCh38
NC_000019.9:g.10226268_10226280del , CM000681.1:g.10226268_10226280del GRCh37
NC_000019.8:g.10087268_10087280del NCBI36
NG_047007.1:g.9072_9084del
NG_051197.1:g.9324_9336del

Transcript Alleles

HGVS Amino-acid Change
ENST00000253108.9:c.841-16_841-4del MANE Select ENSP00000253108.3:n.841-16_841-4del
ENST00000253108.8:c.841-16_841-4del ENSP00000253108.3:n.841-16_841-4del
ENST00000589454.5:c.817-16_817-4del ENSP00000466860.1:n.817-16_817-4del
ENST00000590158.1:n.860-16_860-4del
ENST00000593054.5:c.235-16_235-4del ENSP00000467187.1:n.235-16_235-4del
NM_003755.3:c.841-16_841-4del NP_003746.2:n.841-16_841-4del
NM_003755.4:c.841-16_841-4del NP_003746.2:n.841-16_841-4del
NM_003755.5:c.841-16_841-4del MANE Select NP_003746.2:n.841-16_841-4del