Canonical Allele Identifier: CA409651578

Gene: EEF1A2

Linked Data

• dbSNP Id: rs2082414765
• MyVariant Identifiers: chr20:g.62127357A>C (hg19) ; chr20:g.63496004A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63496004A>C , CM000682.2:g.63496004A>C	GRCh38
NC_000020.10:g.62127357A>C , CM000682.1:g.62127357A>C	GRCh37
NC_000020.9:g.61597801A>C	NCBI36
NG_034083.1:g.8312T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706948.1:c.176T>G	ENSP00000516668.1:p.Val59Gly
ENST00000706949.1:c.176T>G	ENSP00000516669.1:p.Val59Gly
ENST00000217182.6:c.176T>G MANE Select	ENSP00000217182.3:p.Val59Gly
ENST00000298049.12:c.176T>G	ENSP00000298049.8:p.Val59Gly
ENST00000642899.1:c.176T>G	ENSP00000493767.1:p.Val59Gly
ENST00000645357.1:c.176T>G	ENSP00000494971.1:p.Val59Gly
ENST00000645586.1:n.2745T>G
ENST00000646335.1:c.176T>G	ENSP00000494752.1:p.Val59Gly
ENST00000675519.1:c.*48T>G	ENSP00000501859.1:n.*48T>G
ENST00000217182.4:c.176T>G	ENSP00000217182.3:p.Val59Gly
ENST00000298049.11:c.176T>G	ENSP00000298049.7:p.Val59Gly
NM_001958.3:c.176T>G	NP_001949.1:p.Val59Gly
NM_001958.4:c.176T>G	NP_001949.1:p.Val59Gly
NM_001958.5:c.176T>G MANE Select	NP_001949.1:p.Val59Gly