Canonical Allele Identifier: CA2552640657

Gene: EEF1A2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63495942_63495943del , CM000682.2:g.63495942_63495943del	GRCh38
NC_000020.10:g.62127295_62127296del , CM000682.1:g.62127295_62127296del	GRCh37
NC_000020.9:g.61597739_61597740del	NCBI36
NG_034083.1:g.8373_8374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706948.1:c.237_238del	ENSP00000516668.1:p.Lys79AsnfsTer?
ENST00000706949.1:c.237_238del	ENSP00000516669.1:p.Lys79AsnfsTer?
ENST00000217182.6:c.237_238del MANE Select	ENSP00000217182.3:p.Lys79AsnfsTer?
ENST00000298049.12:c.237_238del	ENSP00000298049.8:p.Lys79AsnfsTer?
ENST00000642899.1:c.237_238del	ENSP00000493767.1:p.Lys79AsnfsTer?
ENST00000645357.1:c.237_238del	ENSP00000494971.1:p.Lys79AsnfsTer?
ENST00000645586.1:n.2806_2807del
ENST00000646335.1:c.237_238del	ENSP00000494752.1:p.Lys79AsnfsTer?
ENST00000675519.1:c.*109_*110del	ENSP00000501859.1:n.*109_*110del
ENST00000217182.4:c.237_238del	ENSP00000217182.3:p.Lys79AsnfsTer?
ENST00000298049.11:c.237_238del	ENSP00000298049.7:p.Lys79AsnfsTer?
NM_001958.3:c.237_238del	NP_001949.1:p.Lys79AsnfsTer?
NM_001958.4:c.237_238del	NP_001949.1:p.Lys79AsnfsTer?
NM_001958.5:c.237_238del MANE Select	NP_001949.1:p.Lys79AsnfsTer?