Canonical Allele Identifier: CA1939906989
Gene: EIF3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119050491C= , CM000672.2:g.119050491C= GRCh38
NC_000010.10:g.120810003C= , CM000672.1:g.120810003C= GRCh37
NC_000010.9:g.120799993C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369144.8:c.2473+30G= MANE Select ENSP00000358140.3:n.2473+30G=
ENST00000369144.7:c.2473+30G= ENSP00000358140.3:n.2473+30G=
ENST00000541549.2:c.2473+30G= ENSP00000438178.2:n.2473+30G=
NM_003750.2:c.2473+30G= NP_003741.1:n.2473+30G=
NM_003750.3:c.2473+30G= NP_003741.1:n.2473+30G=
NM_003750.4:c.2473+30G= MANE Select NP_003741.1:n.2473+30G=