Canonical Allele Identifier: CA409651541

Gene: EEF1A2

Linked Data

• MyVariant Identifiers: chr20:g.62127340C>A (hg19) ; chr20:g.63495987C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63495987C>A , CM000682.2:g.63495987C>A	GRCh38
NC_000020.10:g.62127340C>A , CM000682.1:g.62127340C>A	GRCh37
NC_000020.9:g.61597784C>A	NCBI36
NG_034083.1:g.8329G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706948.1:c.193G>T	ENSP00000516668.1:p.Ala65Ser
ENST00000706949.1:c.193G>T	ENSP00000516669.1:p.Ala65Ser
ENST00000217182.6:c.193G>T MANE Select	ENSP00000217182.3:p.Ala65Ser
ENST00000298049.12:c.193G>T	ENSP00000298049.8:p.Ala65Ser
ENST00000642899.1:c.193G>T	ENSP00000493767.1:p.Ala65Ser
ENST00000645357.1:c.193G>T	ENSP00000494971.1:p.Ala65Ser
ENST00000645586.1:n.2762G>T
ENST00000646335.1:c.193G>T	ENSP00000494752.1:p.Ala65Ser
ENST00000675519.1:c.*65G>T	ENSP00000501859.1:n.*65G>T
ENST00000217182.4:c.193G>T	ENSP00000217182.3:p.Ala65Ser
ENST00000298049.11:c.193G>T	ENSP00000298049.7:p.Ala65Ser
NM_001958.3:c.193G>T	NP_001949.1:p.Ala65Ser
NM_001958.4:c.193G>T	NP_001949.1:p.Ala65Ser
NM_001958.5:c.193G>T MANE Select	NP_001949.1:p.Ala65Ser