Canonical Allele Identifier: CA399815833

Gene: EFTUD2

Linked Data

• MyVariant Identifiers: chr17:g.42945182A>T (hg19) ; chr17:g.44867814A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44867814A>T , CM000679.2:g.44867814A>T	GRCh38
NC_000017.10:g.42945182A>T , CM000679.1:g.42945182A>T	GRCh37
NC_000017.9:g.40300708A>T	NCBI36
NG_032674.1:g.36812T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000426333.7:c.1142T>A MANE Select	ENSP00000392094.1:p.Leu381His
ENST00000402521.7:c.1037T>A	ENSP00000385873.2:p.Leu346His
ENST00000426333.6:c.1142T>A	ENSP00000392094.1:p.Leu381His
ENST00000586654.5:n.197T>A
ENST00000590367.5:n.870T>A
ENST00000591382.5:c.1142T>A	ENSP00000467805.1:p.Leu381His
ENST00000591856.1:c.263T>A	ENSP00000468284.1:n.263T>A
ENST00000592576.5:c.1112T>A	ENSP00000465058.1:p.Leu371His
NM_001142605.1:c.1037T>A	NP_001136077.1:p.Leu346His
NM_001258353.1:c.1142T>A	NP_001245282.1:p.Leu381His
NM_001258354.1:c.1112T>A	NP_001245283.1:p.Leu371His
NM_004247.3:c.1142T>A	NP_004238.3:p.Leu381His
XR_934602.1:n.1227T>A
XR_934602.3:n.1223T>A
NM_004247.4:c.1142T>A MANE Select	NP_004238.3:p.Leu381His
NM_001142605.2:c.1037T>A	NP_001136077.1:p.Leu346His
NM_001258353.2:c.1142T>A	NP_001245282.1:p.Leu381His
NM_001258354.2:c.1112T>A	NP_001245283.1:p.Leu371His