Canonical Allele Identifier: CA399811724
Gene: EFTUD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44859913T>A , CM000679.2:g.44859913T>A GRCh38
NC_000017.10:g.42937281T>A , CM000679.1:g.42937281T>A GRCh37
NC_000017.9:g.40292807T>A NCBI36
NG_032674.1:g.44713A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000426333.7:c.1852A>T MANE Select ENSP00000392094.1:p.Thr618Ser
ENST00000402521.7:c.1747A>T ENSP00000385873.2:p.Thr583Ser
ENST00000426333.6:c.1852A>T ENSP00000392094.1:p.Thr618Ser
ENST00000586276.5:n.1514A>T
ENST00000590367.5:n.1580A>T
ENST00000591382.5:c.1852A>T ENSP00000467805.1:p.Thr618Ser
ENST00000592576.5:c.1822A>T ENSP00000465058.1:p.Thr608Ser
NM_001142605.1:c.1747A>T NP_001136077.1:p.Thr583Ser
NM_001258353.1:c.1852A>T NP_001245282.1:p.Thr618Ser
NM_001258354.1:c.1822A>T NP_001245283.1:p.Thr608Ser
NM_004247.3:c.1852A>T NP_004238.3:p.Thr618Ser
XR_934602.1:n.1937A>T
XR_934602.3:n.1933A>T
NM_004247.4:c.1852A>T MANE Select NP_004238.3:p.Thr618Ser
NM_001142605.2:c.1747A>T NP_001136077.1:p.Thr583Ser
NM_001258353.2:c.1852A>T NP_001245282.1:p.Thr618Ser
NM_001258354.2:c.1822A>T NP_001245283.1:p.Thr608Ser