Canonical Allele Identifier: CA2374819712
Gene: EEF1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63488308G= , CM000682.2:g.63488308G= GRCh38
NC_000020.10:g.62119661G= , CM000682.1:g.62119661G= GRCh37
NC_000020.9:g.61590105G= NCBI36
NG_034083.1:g.16008C=

Transcript Alleles

HGVS Amino-acid Change
NM_001958.5:c.1382C= MANE Select NP_001949.1:p.Ala461=
ENST00000217182.6:c.1382C= MANE Select ENSP00000217182.3:p.Ala461=
NM_001958.3:c.1382C= NP_001949.1:p.Ala461=
NM_001958.4:c.1382C= NP_001949.1:p.Ala461=
ENST00000217182.4:c.1382C= ENSP00000217182.3:p.Ala461=
ENST00000298049.11:c.1382C= ENSP00000298049.7:p.Ala461=
ENST00000298049.12:c.1350+32C= ENSP00000298049.8:n.1350+32C=
ENST00000675519.1:c.*1254C= ENSP00000501859.1:n.*1254C=
ENST00000706948.1:c.1340C= ENSP00000516668.1:p.Ala447=
ENST00000706949.1:c.1380+2C= ENSP00000516669.1:n.1380+2C=