Canonical Allele Identifier: CA2813565538

Gene: EIF3G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.10115462_10115463insCGTATCATTAAAAA , CM000681.2:g.10115462_10115463insCGTATCATTAAAAA	GRCh38
NC_000019.9:g.10226138_10226139insCGTATCATTAAAAA , CM000681.1:g.10226138_10226139insCGTATCATTAAAAA	GRCh37
NC_000019.8:g.10087138_10087139insCGTATCATTAAAAA	NCBI36
NG_047007.1:g.8942_8943insCGTATCATTAAAAA
NG_051197.1:g.9462_9463insTTTTTAATGATACG

Transcript Alleles

HGVS	Amino-acid change
ENST00000253108.9:c.947+16_947+17insTTTTTAATGATACG MANE Select	ENSP00000253108.3:n.947+16_947+17insTTTTTAATGATACG
ENST00000253108.8:c.947+16_947+17insTTTTTAATGATACG	ENSP00000253108.3:n.947+16_947+17insTTTTTAATGATACG
ENST00000590158.1:n.966+16_966+17insTTTTTAATGATACG
ENST00000593054.5:c.341+16_341+17insTTTTTAATGATACG	ENSP00000467187.1:n.341+16_341+17insTTTTTAATGATACG
NM_003755.3:c.947+16_947+17insTTTTTAATGATACG	NP_003746.2:n.947+16_947+17insTTTTTAATGATACG
NM_003755.4:c.947+16_947+17insTTTTTAATGATACG	NP_003746.2:n.947+16_947+17insTTTTTAATGATACG
NM_003755.5:c.947+16_947+17insTTTTTAATGATACG MANE Select	NP_003746.2:n.947+16_947+17insTTTTTAATGATACG