Canonical Allele Identifier: CA16620454

Gene: EFTUD2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44857158C>A , CM000679.2:g.44857158C>A	GRCh38
NC_000017.10:g.42934526C>A , CM000679.1:g.42934526C>A	GRCh37
NC_000017.9:g.40290052C>A	NCBI36
NG_032674.1:g.47468G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.1963-1G>T MANE Select	ENSP00000392094.1:n.1963-1G>T
ENST00000402521.7:c.1858-1G>T	ENSP00000385873.2:n.1858-1G>T
ENST00000426333.6:c.1963-1G>T	ENSP00000392094.1:n.1963-1G>T
ENST00000586276.5:n.1625-1G>T
ENST00000588340.1:n.482G>T
ENST00000590367.5:n.1691-1G>T
ENST00000590977.5:n.571-1G>T
ENST00000591382.5:c.1963-1G>T	ENSP00000467805.1:n.1963-1G>T
ENST00000592576.5:c.1933-1G>T	ENSP00000465058.1:n.1933-1G>T
NM_001142605.1:c.1858-1G>T	NP_001136077.1:n.1858-1G>T
NM_001258353.1:c.1963-1G>T	NP_001245282.1:n.1963-1G>T
NM_001258354.1:c.1933-1G>T	NP_001245283.1:n.1933-1G>T
NM_004247.3:c.1963-1G>T	NP_004238.3:n.1963-1G>T
XR_934602.1:n.2048-1G>T
XR_934602.3:n.2044-1G>T
NM_004247.4:c.1963-1G>T MANE Select	NP_004238.3:n.1963-1G>T
NM_001142605.2:c.1858-1G>T	NP_001136077.1:n.1858-1G>T
NM_001258353.2:c.1963-1G>T	NP_001245282.1:n.1963-1G>T
NM_001258354.2:c.1933-1G>T	NP_001245283.1:n.1933-1G>T