Canonical Allele Identifier: CA2261586500

Gene: EFTUD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44854879T= , CM000679.2:g.44854879T=	GRCh38
NC_000017.10:g.42932247T= , CM000679.1:g.42932247T=	GRCh37
NC_000017.9:g.40287773T=	NCBI36
NG_032674.1:g.49747A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.2132+39A= MANE Select	ENSP00000392094.1:n.2132+39A=
ENST00000402521.7:c.2027+39A=	ENSP00000385873.2:n.2027+39A=
ENST00000426333.6:c.2132+39A=	ENSP00000392094.1:n.2132+39A=
ENST00000586276.5:n.1794+39A=
ENST00000590124.5:c.134+39A=	ENSP00000467249.1:n.134+39A=
ENST00000590367.5:n.1860+39A=
ENST00000590977.5:n.740+39A=
ENST00000591382.5:c.2132+39A=	ENSP00000467805.1:n.2132+39A=
ENST00000592576.5:c.2102+39A=	ENSP00000465058.1:n.2102+39A=
NM_001142605.1:c.2027+39A=	NP_001136077.1:n.2027+39A=
NM_001258353.1:c.2132+39A=	NP_001245282.1:n.2132+39A=
NM_001258354.1:c.2102+39A=	NP_001245283.1:n.2102+39A=
NM_004247.3:c.2132+39A=	NP_004238.3:n.2132+39A=
XR_934602.1:n.2217+39A=
XR_934602.3:n.2213+39A=
NM_004247.4:c.2132+39A= MANE Select	NP_004238.3:n.2132+39A=
NM_001142605.2:c.2027+39A=	NP_001136077.1:n.2027+39A=
NM_001258353.2:c.2132+39A=	NP_001245282.1:n.2132+39A=
NM_001258354.2:c.2102+39A=	NP_001245283.1:n.2102+39A=