Canonical Allele Identifier: CA2374824093
Gene: EEF1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63495925G= , CM000682.2:g.63495925G= GRCh38
NC_000020.10:g.62127278G= , CM000682.1:g.62127278G= GRCh37
NC_000020.9:g.61597722G= NCBI36
NG_034083.1:g.8391C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706948.1:c.255C= ENSP00000516668.1:p.Tyr85=
ENST00000706949.1:c.255C= ENSP00000516669.1:p.Tyr85=
ENST00000217182.6:c.255C= MANE Select ENSP00000217182.3:p.Tyr85=
ENST00000298049.12:c.255C= ENSP00000298049.8:p.Tyr85=
ENST00000642899.1:c.255C= ENSP00000493767.1:p.Tyr85=
ENST00000645357.1:c.255C= ENSP00000494971.1:p.Tyr85=
ENST00000645586.1:n.2824C=
ENST00000646335.1:c.255C= ENSP00000494752.1:p.Tyr85=
ENST00000675519.1:c.*127C= ENSP00000501859.1:n.*127C=
ENST00000217182.4:c.255C= ENSP00000217182.3:p.Tyr85=
ENST00000298049.11:c.255C= ENSP00000298049.7:p.Tyr85=
NM_001958.3:c.255C= NP_001949.1:p.Tyr85=
NM_001958.4:c.255C= NP_001949.1:p.Tyr85=
NM_001958.5:c.255C= MANE Select NP_001949.1:p.Tyr85=