Canonical Allele Identifier: CA511340056
Community Standard Title: NM_001958.5(EEF1A2):c.522C>T (p.Val174=)
Gene: EEF1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63494904G>A , CM000682.2:g.63494904G>A GRCh38
NC_000020.10:g.62126257G>A , CM000682.1:g.62126257G>A GRCh37
NC_000020.9:g.61596701G>A NCBI36
NG_034083.1:g.9412C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001958.5:c.522C>T MANE Select NP_001949.1:p.Val174=
ENST00000217182.6:c.522C>T MANE Select ENSP00000217182.3:p.Val174=
NM_001958.3:c.522C>T NP_001949.1:p.Val174=
NM_001958.4:c.522C>T NP_001949.1:p.Val174=
ENST00000217182.4:c.522C>T ENSP00000217182.3:p.Val174=
ENST00000298049.11:c.522C>T ENSP00000298049.7:p.Val174=
ENST00000298049.12:c.522C>T ENSP00000298049.8:p.Val174=
ENST00000645586.1:n.3091C>T
ENST00000675519.1:c.*394C>T ENSP00000501859.1:n.*394C>T
ENST00000706948.1:c.522C>T ENSP00000516668.1:p.Val174=
ENST00000706949.1:c.522C>T ENSP00000516669.1:p.Val174=