Canonical Allele Identifier: CA378286485
Gene: EIF3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.120810090A>T (hg19) chr10:g.119050578A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119050578A>T , CM000672.2:g.119050578A>T GRCh38
NC_000010.10:g.120810090A>T , CM000672.1:g.120810090A>T GRCh37
NC_000010.9:g.120800080A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369144.8:c.2416T>A MANE Select ENSP00000358140.3:p.Tyr806Asn
ENST00000369144.7:c.2416T>A ENSP00000358140.3:p.Tyr806Asn
ENST00000541549.2:c.2416T>A ENSP00000438178.2:p.Tyr806Asn
NM_003750.2:c.2416T>A NP_003741.1:p.Tyr806Asn
NM_003750.3:c.2416T>A NP_003741.1:p.Tyr806Asn
NM_003750.4:c.2416T>A MANE Select NP_003741.1:p.Tyr806Asn
Search 100 bp 5'
Search 100 bp 3'