Canonical Allele Identifier: CA2261585149

Gene: EFTUD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44851763G= , CM000679.2:g.44851763G=	GRCh38
NC_000017.10:g.42929131G= , CM000679.1:g.42929131G=	GRCh37
NC_000017.9:g.40284657G=	NCBI36
NG_032674.1:g.52863C=

Transcript Alleles

HGVS	Amino-acid Change
NM_004247.4:c.2770C= MANE Select	NP_004238.3:p.Gln924=
ENST00000426333.7:c.2770C= MANE Select	ENSP00000392094.1:p.Gln924=
NM_001142605.1:c.2665C=	NP_001136077.1:p.Gln889=
NM_001142605.2:c.2665C=	NP_001136077.1:p.Gln889=
NM_001258353.1:c.2770C=	NP_001245282.1:p.Gln924=
NM_001258353.2:c.2770C=	NP_001245282.1:p.Gln924=
NM_001258354.1:c.2740C=	NP_001245283.1:p.Gln914=
NM_001258354.2:c.2740C=	NP_001245283.1:p.Gln914=
NM_004247.3:c.2770C=	NP_004238.3:p.Gln924=
ENST00000402521.7:c.2665C=	ENSP00000385873.2:p.Gln889=
ENST00000426333.6:c.2770C=	ENSP00000392094.1:p.Gln924=
ENST00000586276.5:n.3065C=
ENST00000589769.1:c.523C=
ENST00000590124.5:c.523C=	ENSP00000467249.1:p.Gln175=
ENST00000590367.5:n.3131C=
ENST00000590977.5:n.1916C=
ENST00000591382.5:c.2770C=	ENSP00000467805.1:p.Gln924=
ENST00000592576.5:c.2740C=	ENSP00000465058.1:p.Gln914=
XR_934602.1:n.2760C=
XR_934602.3:n.2756C=