Canonical Allele Identifier: CA1939907029
Gene: EIF3A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119050573A= , CM000672.2:g.119050573A= GRCh38
NC_000010.10:g.120810085A= , CM000672.1:g.120810085A= GRCh37
NC_000010.9:g.120800075A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369144.8:c.2421T= MANE Select ENSP00000358140.3:p.Tyr807=
ENST00000369144.7:c.2421T= ENSP00000358140.3:p.Tyr807=
ENST00000541549.2:c.2421T= ENSP00000438178.2:p.Tyr807=
NM_003750.2:c.2421T= NP_003741.1:p.Tyr807=
NM_003750.3:c.2421T= NP_003741.1:p.Tyr807=
NM_003750.4:c.2421T= MANE Select NP_003741.1:p.Tyr807=