Canonical Allele Identifier: CA399815823

Gene: EFTUD2

Linked Data

• MyVariant Identifiers: chr17:g.42945180C>G (hg19) ; chr17:g.44867812C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44867812C>G , CM000679.2:g.44867812C>G	GRCh38
NC_000017.10:g.42945180C>G , CM000679.1:g.42945180C>G	GRCh37
NC_000017.9:g.40300706C>G	NCBI36
NG_032674.1:g.36814G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.1144G>C MANE Select	ENSP00000392094.1:p.Ala382Pro
ENST00000402521.7:c.1039G>C	ENSP00000385873.2:p.Ala347Pro
ENST00000426333.6:c.1144G>C	ENSP00000392094.1:p.Ala382Pro
ENST00000586654.5:n.199G>C
ENST00000590367.5:n.872G>C
ENST00000591382.5:c.1144G>C	ENSP00000467805.1:p.Ala382Pro
ENST00000591856.1:c.265G>C	ENSP00000468284.1:n.265G>C
ENST00000592576.5:c.1114G>C	ENSP00000465058.1:p.Ala372Pro
NM_001142605.1:c.1039G>C	NP_001136077.1:p.Ala347Pro
NM_001258353.1:c.1144G>C	NP_001245282.1:p.Ala382Pro
NM_001258354.1:c.1114G>C	NP_001245283.1:p.Ala372Pro
NM_004247.3:c.1144G>C	NP_004238.3:p.Ala382Pro
XR_934602.1:n.1229G>C
XR_934602.3:n.1225G>C
NM_004247.4:c.1144G>C MANE Select	NP_004238.3:p.Ala382Pro
NM_001142605.2:c.1039G>C	NP_001136077.1:p.Ala347Pro
NM_001258353.2:c.1144G>C	NP_001245282.1:p.Ala382Pro
NM_001258354.2:c.1114G>C	NP_001245283.1:p.Ala372Pro