Canonical Allele Identifier: CA2816995742

Gene: EEF1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63496071C>G , CM000682.2:g.63496071C>G	GRCh38
NC_000020.10:g.62127424C>G , CM000682.1:g.62127424C>G	GRCh37
NC_000020.9:g.61597868C>G	NCBI36
NG_034083.1:g.8245G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706948.1:c.145-36G>C	ENSP00000516668.1:n.145-36G>C
ENST00000706949.1:c.145-36G>C	ENSP00000516669.1:n.145-36G>C
ENST00000217182.6:c.145-36G>C MANE Select	ENSP00000217182.3:n.145-36G>C
ENST00000298049.12:c.145-36G>C	ENSP00000298049.8:n.145-36G>C
ENST00000642899.1:c.145-36G>C	ENSP00000493767.1:n.145-36G>C
ENST00000645357.1:c.145-36G>C	ENSP00000494971.1:n.145-36G>C
ENST00000645586.1:n.2678G>C
ENST00000646335.1:c.145-36G>C	ENSP00000494752.1:n.145-36G>C
ENST00000675519.1:c.161G>C	ENSP00000501859.1:p.Gly54Ala
ENST00000217182.4:c.145-36G>C	ENSP00000217182.3:n.145-36G>C
ENST00000298049.11:c.145-36G>C	ENSP00000298049.7:n.145-36G>C
NM_001958.3:c.145-36G>C	NP_001949.1:n.145-36G>C
NM_001958.4:c.145-36G>C	NP_001949.1:n.145-36G>C
NM_001958.5:c.145-36G>C MANE Select	NP_001949.1:n.145-36G>C