Canonical Allele Identifier: CA2261592351

Gene: EFTUD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44867860G= , CM000679.2:g.44867860G=	GRCh38
NC_000017.10:g.42945228G= , CM000679.1:g.42945228G=	GRCh37
NC_000017.9:g.40300754G=	NCBI36
NG_032674.1:g.36766C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000426333.7:c.1096C= MANE Select	ENSP00000392094.1:p.Gln366=
ENST00000402521.7:c.991C=	ENSP00000385873.2:p.Gln331=
ENST00000426333.6:c.1096C=	ENSP00000392094.1:p.Gln366=
ENST00000586654.5:n.151C=
ENST00000590367.5:n.824C=
ENST00000591382.5:c.1096C=	ENSP00000467805.1:p.Gln366=
ENST00000591856.1:c.217C=	ENSP00000468284.1:n.217C=
ENST00000592576.5:c.1066C=	ENSP00000465058.1:p.Gln356=
NM_001142605.1:c.991C=	NP_001136077.1:p.Gln331=
NM_001258353.1:c.1096C=	NP_001245282.1:p.Gln366=
NM_001258354.1:c.1066C=	NP_001245283.1:p.Gln356=
NM_004247.3:c.1096C=	NP_004238.3:p.Gln366=
XR_934602.1:n.1181C=
XR_934602.3:n.1177C=
NM_004247.4:c.1096C= MANE Select	NP_004238.3:p.Gln366=
NM_001142605.2:c.991C=	NP_001136077.1:p.Gln331=
NM_001258353.2:c.1096C=	NP_001245282.1:p.Gln366=
NM_001258354.2:c.1066C=	NP_001245283.1:p.Gln356=