Canonical Allele Identifier: CA2813565531
Gene: EIF3G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.10115431_10115432insTAGAT , CM000681.2:g.10115431_10115432insTAGAT GRCh38
NC_000019.9:g.10226107_10226108insTAGAT , CM000681.1:g.10226107_10226108insTAGAT GRCh37
NC_000019.8:g.10087107_10087108insTAGAT NCBI36
NG_047007.1:g.8911_8912insTAGAT
NG_051197.1:g.9493_9494insATCTA

Transcript Alleles

HGVS Amino-acid change
ENST00000253108.9:c.947+47_947+48insATCTA MANE Select ENSP00000253108.3:n.947+47_947+48insATCTA
ENST00000253108.8:c.947+47_947+48insATCTA ENSP00000253108.3:n.947+47_947+48insATCTA
ENST00000590158.1:n.966+47_966+48insATCTA
ENST00000593054.5:c.341+47_341+48insATCTA ENSP00000467187.1:n.341+47_341+48insATCTA
NM_003755.3:c.947+47_947+48insATCTA NP_003746.2:n.947+47_947+48insATCTA
NM_003755.4:c.947+47_947+48insATCTA NP_003746.2:n.947+47_947+48insATCTA
NM_003755.5:c.947+47_947+48insATCTA MANE Select NP_003746.2:n.947+47_947+48insATCTA