Canonical Allele Identifier: CA500318705

Gene: EFTUD2

Linked Data

• MyVariant Identifiers: chr17:g.42963954T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44886586T>C , CM000679.2:g.44886586T>C	GRCh38
NC_000017.10:g.42963954T>C , CM000679.1:g.42963954T>C	GRCh37
NC_000017.9:g.40319480T>C	NCBI36
NG_032674.1:g.18040A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000426333.7:c.270A>G MANE Select	ENSP00000392094.1:p.Thr90=
ENST00000402521.7:c.165A>G	ENSP00000385873.2:p.Thr55=
ENST00000426333.6:c.270A>G	ENSP00000392094.1:p.Thr90=
ENST00000588374.1:c.82-1252A>G	ENSP00000467639.1:n.82-1252A>G
ENST00000589825.5:n.351A>G
ENST00000591382.5:c.270A>G	ENSP00000467805.1:p.Thr90=
ENST00000592408.5:n.481A>G
ENST00000592576.5:c.270A>G	ENSP00000465058.1:p.Thr90=
ENST00000592701.2:c.270A>G	ENSP00000464908.1:p.Thr90=
ENST00000593072.5:c.270A>G	ENSP00000464882.1:p.Thr90=
NM_001142605.1:c.165A>G	NP_001136077.1:p.Thr55=
NM_001258353.1:c.270A>G	NP_001245282.1:p.Thr90=
NM_001258354.1:c.270A>G	NP_001245283.1:p.Thr90=
NM_004247.3:c.270A>G	NP_004238.3:p.Thr90=
XR_934602.1:n.355A>G
XR_934602.3:n.351A>G
NM_004247.4:c.270A>G MANE Select	NP_004238.3:p.Thr90=
NM_001142605.2:c.165A>G	NP_001136077.1:p.Thr55=
NM_001258353.2:c.270A>G	NP_001245282.1:p.Thr90=
NM_001258354.2:c.270A>G	NP_001245283.1:p.Thr90=