Canonical Allele Identifier: CA399826471

Gene: EFTUD2

Linked Data

• MyVariant Identifiers: chr17:g.42964027T>G (hg19) ; chr17:g.44886659T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44886659T>G , CM000679.2:g.44886659T>G	GRCh38
NC_000017.10:g.42964027T>G , CM000679.1:g.42964027T>G	GRCh37
NC_000017.9:g.40319553T>G	NCBI36
NG_032674.1:g.17967A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.197A>C MANE Select	ENSP00000392094.1:p.Tyr66Ser
ENST00000402521.7:c.92A>C	ENSP00000385873.2:p.Tyr31Ser
ENST00000426333.6:c.197A>C	ENSP00000392094.1:p.Tyr66Ser
ENST00000588374.1:c.82-1325A>C	ENSP00000467639.1:n.82-1325A>C
ENST00000589825.5:n.278A>C
ENST00000591382.5:c.197A>C	ENSP00000467805.1:p.Tyr66Ser
ENST00000592408.5:n.408A>C
ENST00000592576.5:c.197A>C	ENSP00000465058.1:p.Tyr66Ser
ENST00000592701.2:c.197A>C	ENSP00000464908.1:p.Tyr66Ser
ENST00000593072.5:c.197A>C	ENSP00000464882.1:p.Tyr66Ser
NM_001142605.1:c.92A>C	NP_001136077.1:p.Tyr31Ser
NM_001258353.1:c.197A>C	NP_001245282.1:p.Tyr66Ser
NM_001258354.1:c.197A>C	NP_001245283.1:p.Tyr66Ser
NM_004247.3:c.197A>C	NP_004238.3:p.Tyr66Ser
XR_934602.1:n.282A>C
XR_934602.3:n.278A>C
NM_004247.4:c.197A>C MANE Select	NP_004238.3:p.Tyr66Ser
NM_001142605.2:c.92A>C	NP_001136077.1:p.Tyr31Ser
NM_001258353.2:c.197A>C	NP_001245282.1:p.Tyr66Ser
NM_001258354.2:c.197A>C	NP_001245283.1:p.Tyr66Ser