Canonical Allele Identifier: CA2261601065

Gene: EFTUD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44886658G= , CM000679.2:g.44886658G=	GRCh38
NC_000017.10:g.42964026G= , CM000679.1:g.42964026G=	GRCh37
NC_000017.9:g.40319552G=	NCBI36
NG_032674.1:g.17968C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.198C= MANE Select	ENSP00000392094.1:p.Tyr66=
ENST00000402521.7:c.93C=	ENSP00000385873.2:p.Tyr31=
ENST00000426333.6:c.198C=	ENSP00000392094.1:p.Tyr66=
ENST00000588374.1:c.82-1324C=	ENSP00000467639.1:n.82-1324C=
ENST00000589825.5:n.279C=
ENST00000591382.5:c.198C=	ENSP00000467805.1:p.Tyr66=
ENST00000592408.5:n.409C=
ENST00000592576.5:c.198C=	ENSP00000465058.1:p.Tyr66=
ENST00000592701.2:c.198C=	ENSP00000464908.1:p.Tyr66=
ENST00000593072.5:c.198C=	ENSP00000464882.1:p.Tyr66=
NM_001142605.1:c.93C=	NP_001136077.1:p.Tyr31=
NM_001258353.1:c.198C=	NP_001245282.1:p.Tyr66=
NM_001258354.1:c.198C=	NP_001245283.1:p.Tyr66=
NM_004247.3:c.198C=	NP_004238.3:p.Tyr66=
XR_934602.1:n.283C=
XR_934602.3:n.279C=
NM_004247.4:c.198C= MANE Select	NP_004238.3:p.Tyr66=
NM_001142605.2:c.93C=	NP_001136077.1:p.Tyr31=
NM_001258353.2:c.198C=	NP_001245282.1:p.Tyr66=
NM_001258354.2:c.198C=	NP_001245283.1:p.Tyr66=