Canonical Allele Identifier: CA409651399

Gene: EEF1A2

Linked Data

• ClinVar Variation Id: 488944
• ClinVar RCV Id: RCV000578921
• dbSNP Id: rs1555883865
• MyVariant Identifiers: chr20:g.62127278G>C (hg19) ; chr20:g.63495925G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706948.1:c.255C>G	ENSP00000516668.1:p.Tyr85Ter
ENST00000706949.1:c.255C>G	ENSP00000516669.1:p.Tyr85Ter
ENST00000217182.6:c.255C>G MANE Select	ENSP00000217182.3:p.Tyr85Ter
ENST00000298049.12:c.255C>G	ENSP00000298049.8:p.Tyr85Ter
ENST00000642899.1:c.255C>G	ENSP00000493767.1:p.Tyr85Ter
ENST00000645357.1:c.255C>G	ENSP00000494971.1:p.Tyr85Ter
ENST00000645586.1:n.2824C>G
ENST00000646335.1:c.255C>G	ENSP00000494752.1:p.Tyr85Ter
ENST00000675519.1:c.*127C>G	ENSP00000501859.1:n.*127C>G
ENST00000217182.4:c.255C>G	ENSP00000217182.3:p.Tyr85Ter
ENST00000298049.11:c.255C>G	ENSP00000298049.7:p.Tyr85Ter
NM_001958.3:c.255C>G	NP_001949.1:p.Tyr85Ter
NM_001958.4:c.255C>G	NP_001949.1:p.Tyr85Ter
NM_001958.5:c.255C>G MANE Select	NP_001949.1:p.Tyr85Ter