Canonical Allele Identifier: CA2813565536
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115459_10115460insT , CM000681.2:g.10115459_10115460insT GRCh38
NC_000019.9:g.10226135_10226136insT , CM000681.1:g.10226135_10226136insT GRCh37
NC_000019.8:g.10087135_10087136insT NCBI36
NG_047007.1:g.8939_8940insT
NG_051197.1:g.9465_9466insA

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+19_947+20insA MANE Select ENSP00000253108.3:n.947+19_947+20insA
ENST00000253108.8:c.947+19_947+20insA ENSP00000253108.3:n.947+19_947+20insA
ENST00000590158.1:n.966+19_966+20insA
ENST00000593054.5:c.341+19_341+20insA ENSP00000467187.1:n.341+19_341+20insA
NM_003755.3:c.947+19_947+20insA NP_003746.2:n.947+19_947+20insA
NM_003755.4:c.947+19_947+20insA NP_003746.2:n.947+19_947+20insA
NM_003755.5:c.947+19_947+20insA MANE Select NP_003746.2:n.947+19_947+20insA