Canonical Allele Identifier: CA399844042

Gene: EFTUD2

Linked Data

• MyVariant Identifiers: chr17:g.42932362T>C (hg19) ; chr17:g.44854994T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44854994T>C , CM000679.2:g.44854994T>C	GRCh38
NC_000017.10:g.42932362T>C , CM000679.1:g.42932362T>C	GRCh37
NC_000017.9:g.40287888T>C	NCBI36
NG_032674.1:g.49632A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.2056A>G MANE Select	ENSP00000392094.1:p.Thr686Ala
ENST00000402521.7:c.1951A>G	ENSP00000385873.2:p.Thr651Ala
ENST00000426333.6:c.2056A>G	ENSP00000392094.1:p.Thr686Ala
ENST00000586276.5:n.1718A>G
ENST00000588340.1:n.576A>G
ENST00000590124.5:c.58A>G	ENSP00000467249.1:p.Thr20Ala
ENST00000590367.5:n.1784A>G
ENST00000590977.5:n.664A>G
ENST00000591382.5:c.2056A>G	ENSP00000467805.1:p.Thr686Ala
ENST00000592576.5:c.2026A>G	ENSP00000465058.1:p.Thr676Ala
NM_001142605.1:c.1951A>G	NP_001136077.1:p.Thr651Ala
NM_001258353.1:c.2056A>G	NP_001245282.1:p.Thr686Ala
NM_001258354.1:c.2026A>G	NP_001245283.1:p.Thr676Ala
NM_004247.3:c.2056A>G	NP_004238.3:p.Thr686Ala
XR_934602.1:n.2141A>G
XR_934602.3:n.2137A>G
NM_004247.4:c.2056A>G MANE Select	NP_004238.3:p.Thr686Ala
NM_001142605.2:c.1951A>G	NP_001136077.1:p.Thr651Ala
NM_001258353.2:c.2056A>G	NP_001245282.1:p.Thr686Ala
NM_001258354.2:c.2026A>G	NP_001245283.1:p.Thr676Ala