Canonical Allele Identifier: CA378286474
Gene: EIF3A HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.120810088G>C (hg19) chr10:g.119050576G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.119050576G>C , CM000672.2:g.119050576G>C GRCh38
NC_000010.10:g.120810088G>C , CM000672.1:g.120810088G>C GRCh37
NC_000010.9:g.120800078G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369144.8:c.2418C>G MANE Select ENSP00000358140.3:p.Tyr806Ter
ENST00000369144.7:c.2418C>G ENSP00000358140.3:p.Tyr806Ter
ENST00000541549.2:c.2418C>G ENSP00000438178.2:p.Tyr806Ter
NM_003750.2:c.2418C>G NP_003741.1:p.Tyr806Ter
NM_003750.3:c.2418C>G NP_003741.1:p.Tyr806Ter
NM_003750.4:c.2418C>G MANE Select NP_003741.1:p.Tyr806Ter
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