Canonical Allele Identifier: CA399816075

Gene: EFTUD2

Linked Data

• MyVariant Identifiers: chr17:g.42945242G>C (hg19) ; chr17:g.44867874G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44867874G>C , CM000679.2:g.44867874G>C	GRCh38
NC_000017.10:g.42945242G>C , CM000679.1:g.42945242G>C	GRCh37
NC_000017.9:g.40300768G>C	NCBI36
NG_032674.1:g.36752C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.1082C>G MANE Select	ENSP00000392094.1:p.Pro361Arg
ENST00000402521.7:c.977C>G	ENSP00000385873.2:p.Pro326Arg
ENST00000426333.6:c.1082C>G	ENSP00000392094.1:p.Pro361Arg
ENST00000586654.5:n.137C>G
ENST00000590367.5:n.810C>G
ENST00000591382.5:c.1082C>G	ENSP00000467805.1:p.Pro361Arg
ENST00000591856.1:c.203C>G	ENSP00000468284.1:n.203C>G
ENST00000592576.5:c.1052C>G	ENSP00000465058.1:p.Pro351Arg
NM_001142605.1:c.977C>G	NP_001136077.1:p.Pro326Arg
NM_001258353.1:c.1082C>G	NP_001245282.1:p.Pro361Arg
NM_001258354.1:c.1052C>G	NP_001245283.1:p.Pro351Arg
NM_004247.3:c.1082C>G	NP_004238.3:p.Pro361Arg
XR_934602.1:n.1167C>G
XR_934602.3:n.1163C>G
NM_004247.4:c.1082C>G MANE Select	NP_004238.3:p.Pro361Arg
NM_001142605.2:c.977C>G	NP_001136077.1:p.Pro326Arg
NM_001258353.2:c.1082C>G	NP_001245282.1:p.Pro361Arg
NM_001258354.2:c.1052C>G	NP_001245283.1:p.Pro351Arg