Canonical Allele Identifier: CA471628828

Gene: EIF3A

Linked Data

• dbSNP Id: rs2119818670
• MyVariant Identifiers: chr10:g.120810055C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.119050543C>T , CM000672.2:g.119050543C>T	GRCh38
NC_000010.10:g.120810055C>T , CM000672.1:g.120810055C>T	GRCh37
NC_000010.9:g.120800045C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369144.8:c.2451G>A MANE Select	ENSP00000358140.3:p.Arg817=
ENST00000369144.7:c.2451G>A	ENSP00000358140.3:p.Arg817=
ENST00000541549.2:c.2451G>A	ENSP00000438178.2:p.Arg817=
NM_003750.2:c.2451G>A	NP_003741.1:p.Arg817=
NM_003750.3:c.2451G>A	NP_003741.1:p.Arg817=
NM_003750.4:c.2451G>A MANE Select	NP_003741.1:p.Arg817=