Canonical Allele Identifier: CA500312302

Gene: EFTUD2

Linked Data

• MyVariant Identifiers: chr17:g.42932297A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44854929A>G , CM000679.2:g.44854929A>G	GRCh38
NC_000017.10:g.42932297A>G , CM000679.1:g.42932297A>G	GRCh37
NC_000017.9:g.40287823A>G	NCBI36
NG_032674.1:g.49697T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.2121T>C MANE Select	ENSP00000392094.1:p.Ile707=
ENST00000402521.7:c.2016T>C	ENSP00000385873.2:p.Ile672=
ENST00000426333.6:c.2121T>C	ENSP00000392094.1:p.Ile707=
ENST00000586276.5:n.1783T>C
ENST00000590124.5:c.123T>C	ENSP00000467249.1:p.Ile41=
ENST00000590367.5:n.1849T>C
ENST00000590977.5:n.729T>C
ENST00000591382.5:c.2121T>C	ENSP00000467805.1:p.Ile707=
ENST00000592576.5:c.2091T>C	ENSP00000465058.1:p.Ile697=
NM_001142605.1:c.2016T>C	NP_001136077.1:p.Ile672=
NM_001258353.1:c.2121T>C	NP_001245282.1:p.Ile707=
NM_001258354.1:c.2091T>C	NP_001245283.1:p.Ile697=
NM_004247.3:c.2121T>C	NP_004238.3:p.Ile707=
XR_934602.1:n.2206T>C
XR_934602.3:n.2202T>C
NM_004247.4:c.2121T>C MANE Select	NP_004238.3:p.Ile707=
NM_001142605.2:c.2016T>C	NP_001136077.1:p.Ile672=
NM_001258353.2:c.2121T>C	NP_001245282.1:p.Ile707=
NM_001258354.2:c.2091T>C	NP_001245283.1:p.Ile697=