Canonical Allele Identifier: CA511204022

Gene: EEF1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63488334G>C , CM000682.2:g.63488334G>C	GRCh38
NC_000020.10:g.62119687G>C , CM000682.1:g.62119687G>C	GRCh37
NC_000020.9:g.61590131G>C	NCBI36
NG_034083.1:g.15982C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001958.5:c.1356C>G MANE Select	NP_001949.1:p.Thr452=
ENST00000217182.6:c.1356C>G MANE Select	ENSP00000217182.3:p.Thr452=
NM_001958.3:c.1356C>G	NP_001949.1:p.Thr452=
NM_001958.4:c.1356C>G	NP_001949.1:p.Thr452=
ENST00000217182.4:c.1356C>G	ENSP00000217182.3:p.Thr452=
ENST00000298049.11:c.1356C>G	ENSP00000298049.7:p.Thr452=
ENST00000298049.12:c.1350+6C>G	ENSP00000298049.8:n.1350+6C>G
ENST00000675519.1:c.*1228C>G	ENSP00000501859.1:n.*1228C>G
ENST00000706948.1:c.1314C>G	ENSP00000516668.1:p.Thr438=
ENST00000706949.1:c.1356C>G	ENSP00000516669.1:p.Thr452=