Canonical Allele Identifier: CA2813565534
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115437_10115456del , CM000681.2:g.10115437_10115456del GRCh38
NC_000019.9:g.10226113_10226132del , CM000681.1:g.10226113_10226132del GRCh37
NC_000019.8:g.10087113_10087132del NCBI36
NG_047007.1:g.8917_8936del
NG_051197.1:g.9469_9488del

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+23_947+42del MANE Select ENSP00000253108.3:n.947+23_947+42del
ENST00000253108.8:c.947+23_947+42del ENSP00000253108.3:n.947+23_947+42del
ENST00000590158.1:n.966+23_966+42del
ENST00000593054.5:c.341+23_341+42del ENSP00000467187.1:n.341+23_341+42del
NM_003755.3:c.947+23_947+42del NP_003746.2:n.947+23_947+42del
NM_003755.4:c.947+23_947+42del NP_003746.2:n.947+23_947+42del
NM_003755.5:c.947+23_947+42del MANE Select NP_003746.2:n.947+23_947+42del