Canonical Allele Identifier: CA2374823987

Gene: EEF1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63495715G= , CM000682.2:g.63495715G=	GRCh38
NC_000020.10:g.62127068G= , CM000682.1:g.62127068G=	GRCh37
NC_000020.9:g.61597512G=	NCBI36
NG_034083.1:g.8601C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706948.1:c.324+141C=	ENSP00000516668.1:n.324+141C=
ENST00000706949.1:c.324+141C=	ENSP00000516669.1:n.324+141C=
ENST00000217182.6:c.324+141C= MANE Select	ENSP00000217182.3:n.324+141C=
ENST00000298049.12:c.324+141C=	ENSP00000298049.8:n.324+141C=
ENST00000642899.1:c.324+141C=	ENSP00000493767.1:n.324+141C=
ENST00000645357.1:c.324+141C=	ENSP00000494971.1:n.324+141C=
ENST00000645586.1:n.2893+141C=
ENST00000675519.1:c.*196+141C=	ENSP00000501859.1:n.*196+141C=
ENST00000217182.4:c.324+141C=	ENSP00000217182.3:n.324+141C=
ENST00000298049.11:c.324+141C=	ENSP00000298049.7:n.324+141C=
NM_001958.3:c.324+141C=	NP_001949.1:n.324+141C=
NM_001958.4:c.324+141C=	NP_001949.1:n.324+141C=
NM_001958.5:c.324+141C= MANE Select	NP_001949.1:n.324+141C=