Canonical Allele Identifier: CA2261586570

Gene: EFTUD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44855041C= , CM000679.2:g.44855041C=	GRCh38
NC_000017.10:g.42932409C= , CM000679.1:g.42932409C=	GRCh37
NC_000017.9:g.40287935C=	NCBI36
NG_032674.1:g.49585G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.2046-37G= MANE Select	ENSP00000392094.1:n.2046-37G=
ENST00000402521.7:c.1941-37G=	ENSP00000385873.2:n.1941-37G=
ENST00000426333.6:c.2046-37G=	ENSP00000392094.1:n.2046-37G=
ENST00000586276.5:n.1708-37G=
ENST00000588340.1:n.566-37G=
ENST00000590124.5:c.48-37G=	ENSP00000467249.1:n.48-37G=
ENST00000590367.5:n.1774-37G=
ENST00000590977.5:n.654-37G=
ENST00000591382.5:c.2046-37G=	ENSP00000467805.1:n.2046-37G=
ENST00000592576.5:c.2016-37G=	ENSP00000465058.1:n.2016-37G=
NM_001142605.1:c.1941-37G=	NP_001136077.1:n.1941-37G=
NM_001258353.1:c.2046-37G=	NP_001245282.1:n.2046-37G=
NM_001258354.1:c.2016-37G=	NP_001245283.1:n.2016-37G=
NM_004247.3:c.2046-37G=	NP_004238.3:n.2046-37G=
XR_934602.1:n.2131-37G=
XR_934602.3:n.2127-37G=
NM_004247.4:c.2046-37G= MANE Select	NP_004238.3:n.2046-37G=
NM_001142605.2:c.1941-37G=	NP_001136077.1:n.1941-37G=
NM_001258353.2:c.2046-37G=	NP_001245282.1:n.2046-37G=
NM_001258354.2:c.2016-37G=	NP_001245283.1:n.2016-37G=