Canonical Allele Identifier: CA399826490

Gene: EFTUD2

Linked Data

• MyVariant Identifiers: chr17:g.42964031A>T (hg19) ; chr17:g.44886663A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44886663A>T , CM000679.2:g.44886663A>T	GRCh38
NC_000017.10:g.42964031A>T , CM000679.1:g.42964031A>T	GRCh37
NC_000017.9:g.40319557A>T	NCBI36
NG_032674.1:g.17963T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.193T>A MANE Select	ENSP00000392094.1:p.Tyr65Asn
ENST00000402521.7:c.88T>A	ENSP00000385873.2:p.Tyr30Asn
ENST00000426333.6:c.193T>A	ENSP00000392094.1:p.Tyr65Asn
ENST00000588374.1:c.82-1329T>A	ENSP00000467639.1:n.82-1329T>A
ENST00000589211.1:n.584T>A
ENST00000589825.5:n.274T>A
ENST00000591382.5:c.193T>A	ENSP00000467805.1:p.Tyr65Asn
ENST00000592408.5:n.404T>A
ENST00000592576.5:c.193T>A	ENSP00000465058.1:p.Tyr65Asn
ENST00000592701.2:c.193T>A	ENSP00000464908.1:p.Tyr65Asn
ENST00000593072.5:c.193T>A	ENSP00000464882.1:p.Tyr65Asn
NM_001142605.1:c.88T>A	NP_001136077.1:p.Tyr30Asn
NM_001258353.1:c.193T>A	NP_001245282.1:p.Tyr65Asn
NM_001258354.1:c.193T>A	NP_001245283.1:p.Tyr65Asn
NM_004247.3:c.193T>A	NP_004238.3:p.Tyr65Asn
XR_934602.1:n.278T>A
XR_934602.3:n.274T>A
NM_004247.4:c.193T>A MANE Select	NP_004238.3:p.Tyr65Asn
NM_001142605.2:c.88T>A	NP_001136077.1:p.Tyr30Asn
NM_001258353.2:c.193T>A	NP_001245282.1:p.Tyr65Asn
NM_001258354.2:c.193T>A	NP_001245283.1:p.Tyr65Asn