Canonical Allele Identifier: CA2261588893

Gene: EFTUD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44859912G= , CM000679.2:g.44859912G=	GRCh38
NC_000017.10:g.42937280G= , CM000679.1:g.42937280G=	GRCh37
NC_000017.9:g.40292806G=	NCBI36
NG_032674.1:g.44714C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.1853C= MANE Select	ENSP00000392094.1:p.Thr618=
ENST00000402521.7:c.1748C=	ENSP00000385873.2:p.Thr583=
ENST00000426333.6:c.1853C=	ENSP00000392094.1:p.Thr618=
ENST00000586276.5:n.1515C=
ENST00000590367.5:n.1581C=
ENST00000591382.5:c.1853C=	ENSP00000467805.1:p.Thr618=
ENST00000592576.5:c.1823C=	ENSP00000465058.1:p.Thr608=
NM_001142605.1:c.1748C=	NP_001136077.1:p.Thr583=
NM_001258353.1:c.1853C=	NP_001245282.1:p.Thr618=
NM_001258354.1:c.1823C=	NP_001245283.1:p.Thr608=
NM_004247.3:c.1853C=	NP_004238.3:p.Thr618=
XR_934602.1:n.1938C=
XR_934602.3:n.1934C=
NM_004247.4:c.1853C= MANE Select	NP_004238.3:p.Thr618=
NM_001142605.2:c.1748C=	NP_001136077.1:p.Thr583=
NM_001258353.2:c.1853C=	NP_001245282.1:p.Thr618=
NM_001258354.2:c.1823C=	NP_001245283.1:p.Thr608=