Canonical Allele Identifier: CA409651530

Gene: EEF1A2

Linked Data

• MyVariant Identifiers: chr20:g.62127335C>A (hg19) ; chr20:g.63495982C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63495982C>A , CM000682.2:g.63495982C>A	GRCh38
NC_000020.10:g.62127335C>A , CM000682.1:g.62127335C>A	GRCh37
NC_000020.9:g.61597779C>A	NCBI36
NG_034083.1:g.8334G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706948.1:c.198G>T	ENSP00000516668.1:p.Glu66Asp
ENST00000706949.1:c.198G>T	ENSP00000516669.1:p.Glu66Asp
ENST00000217182.6:c.198G>T MANE Select	ENSP00000217182.3:p.Glu66Asp
ENST00000298049.12:c.198G>T	ENSP00000298049.8:p.Glu66Asp
ENST00000642899.1:c.198G>T	ENSP00000493767.1:p.Glu66Asp
ENST00000645357.1:c.198G>T	ENSP00000494971.1:p.Glu66Asp
ENST00000645586.1:n.2767G>T
ENST00000646335.1:c.198G>T	ENSP00000494752.1:p.Glu66Asp
ENST00000675519.1:c.*70G>T	ENSP00000501859.1:n.*70G>T
ENST00000217182.4:c.198G>T	ENSP00000217182.3:p.Glu66Asp
ENST00000298049.11:c.198G>T	ENSP00000298049.7:p.Glu66Asp
NM_001958.3:c.198G>T	NP_001949.1:p.Glu66Asp
NM_001958.4:c.198G>T	NP_001949.1:p.Glu66Asp
NM_001958.5:c.198G>T MANE Select	NP_001949.1:p.Glu66Asp