Canonical Allele Identifier: CA16620982
Gene: EEF1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 422192
dbSNP Id: rs1064795618

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63497693G>A , CM000682.2:g.63497693G>A GRCh38
NC_000020.10:g.62129046G>A , CM000682.1:g.62129046G>A GRCh37
NC_000020.9:g.61599490G>A NCBI36
NG_034083.1:g.6623C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000706948.1:c.71C>T ENSP00000516668.1:p.Thr24Met
ENST00000706949.1:c.71C>T ENSP00000516669.1:p.Thr24Met
ENST00000217182.6:c.71C>T MANE Select ENSP00000217182.3:p.Thr24Met
ENST00000298049.12:c.71C>T ENSP00000298049.8:p.Thr24Met
ENST00000642899.1:c.71C>T ENSP00000493767.1:p.Thr24Met
ENST00000643976.1:n.270C>T
ENST00000645357.1:c.71C>T ENSP00000494971.1:p.Thr24Met
ENST00000645586.1:n.1056C>T
ENST00000646335.1:c.71C>T ENSP00000494752.1:p.Thr24Met
ENST00000675519.1:c.71C>T ENSP00000501859.1:p.Thr24Met
ENST00000217182.4:c.71C>T ENSP00000217182.3:p.Thr24Met
ENST00000298049.11:c.71C>T ENSP00000298049.7:p.Thr24Met
NM_001958.3:c.71C>T NP_001949.1:p.Thr24Met
NM_001958.4:c.71C>T NP_001949.1:p.Thr24Met
NM_001958.5:c.71C>T MANE Select NP_001949.1:p.Thr24Met