Canonical Allele Identifier: CA9959179

Gene: EEF1A2

Linked Data

• dbSNP Id: rs780001206
• ExAC: 20:62127414 A / G
• MyVariant Identifiers: chr20:g.62127414A>G (hg19) ; chr20:g.63496061A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63496061A>G , CM000682.2:g.63496061A>G	GRCh38
NC_000020.10:g.62127414A>G , CM000682.1:g.62127414A>G	GRCh37
NC_000020.9:g.61597858A>G	NCBI36
NG_034083.1:g.8255T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706948.1:c.145-26T>C	ENSP00000516668.1:n.145-26T>C
ENST00000706949.1:c.145-26T>C	ENSP00000516669.1:n.145-26T>C
ENST00000217182.6:c.145-26T>C MANE Select	ENSP00000217182.3:n.145-26T>C
ENST00000298049.12:c.145-26T>C	ENSP00000298049.8:n.145-26T>C
ENST00000642899.1:c.145-26T>C	ENSP00000493767.1:n.145-26T>C
ENST00000645357.1:c.145-26T>C	ENSP00000494971.1:n.145-26T>C
ENST00000645586.1:n.2688T>C
ENST00000646335.1:c.145-26T>C	ENSP00000494752.1:n.145-26T>C
ENST00000675519.1:c.171T>C	ENSP00000501859.1:p.Pro57=
ENST00000217182.4:c.145-26T>C	ENSP00000217182.3:n.145-26T>C
ENST00000298049.11:c.145-26T>C	ENSP00000298049.7:n.145-26T>C
NM_001958.3:c.145-26T>C	NP_001949.1:n.145-26T>C
NM_001958.4:c.145-26T>C	NP_001949.1:n.145-26T>C
NM_001958.5:c.145-26T>C MANE Select	NP_001949.1:n.145-26T>C