Canonical Allele Identifier: CA2261592355

Gene: EFTUD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44867869T= , CM000679.2:g.44867869T=	GRCh38
NC_000017.10:g.42945237T= , CM000679.1:g.42945237T=	GRCh37
NC_000017.9:g.40300763T=	NCBI36
NG_032674.1:g.36757A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000426333.7:c.1087A= MANE Select	ENSP00000392094.1:p.Ser363=
ENST00000402521.7:c.982A=	ENSP00000385873.2:p.Ser328=
ENST00000426333.6:c.1087A=	ENSP00000392094.1:p.Ser363=
ENST00000586654.5:n.142A=
ENST00000590367.5:n.815A=
ENST00000591382.5:c.1087A=	ENSP00000467805.1:p.Ser363=
ENST00000591856.1:c.208A=	ENSP00000468284.1:n.208A=
ENST00000592576.5:c.1057A=	ENSP00000465058.1:p.Ser353=
NM_001142605.1:c.982A=	NP_001136077.1:p.Ser328=
NM_001258353.1:c.1087A=	NP_001245282.1:p.Ser363=
NM_001258354.1:c.1057A=	NP_001245283.1:p.Ser353=
NM_004247.3:c.1087A=	NP_004238.3:p.Ser363=
XR_934602.1:n.1172A=
XR_934602.3:n.1168A=
NM_004247.4:c.1087A= MANE Select	NP_004238.3:p.Ser363=
NM_001142605.2:c.982A=	NP_001136077.1:p.Ser328=
NM_001258353.2:c.1087A=	NP_001245282.1:p.Ser363=
NM_001258354.2:c.1057A=	NP_001245283.1:p.Ser353=