Canonical Allele Identifier: CA2374824129

Gene: EEF1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63496030C= , CM000682.2:g.63496030C=	GRCh38
NC_000020.10:g.62127383C= , CM000682.1:g.62127383C=	GRCh37
NC_000020.9:g.61597827C=	NCBI36
NG_034083.1:g.8286G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706948.1:c.150G=	ENSP00000516668.1:p.Gly50=
ENST00000706949.1:c.150G=	ENSP00000516669.1:p.Gly50=
ENST00000217182.6:c.150G= MANE Select	ENSP00000217182.3:p.Gly50=
ENST00000298049.12:c.150G=	ENSP00000298049.8:p.Gly50=
ENST00000642899.1:c.150G=	ENSP00000493767.1:p.Gly50=
ENST00000645357.1:c.150G=	ENSP00000494971.1:p.Gly50=
ENST00000645586.1:n.2719G=
ENST00000646335.1:c.150G=	ENSP00000494752.1:p.Gly50=
ENST00000675519.1:c.*22G=	ENSP00000501859.1:n.*22G=
ENST00000217182.4:c.150G=	ENSP00000217182.3:p.Gly50=
ENST00000298049.11:c.150G=	ENSP00000298049.7:p.Gly50=
NM_001958.3:c.150G=	NP_001949.1:p.Gly50=
NM_001958.4:c.150G=	NP_001949.1:p.Gly50=
NM_001958.5:c.150G= MANE Select	NP_001949.1:p.Gly50=