Canonical Allele Identifier: CA2638263949

Gene: EFTUD2

Linked Data

• gnomAD v4: 17-44867929-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44867929G>T , CM000679.2:g.44867929G>T	GRCh38
NC_000017.10:g.42945297G>T , CM000679.1:g.42945297G>T	GRCh37
NC_000017.9:g.40300823G>T	NCBI36
NG_032674.1:g.36697C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.1059-32C>A MANE Select	ENSP00000392094.1:n.1059-32C>A
ENST00000402521.7:c.954-32C>A	ENSP00000385873.2:n.954-32C>A
ENST00000426333.6:c.1059-32C>A	ENSP00000392094.1:n.1059-32C>A
ENST00000586654.5:n.114-32C>A
ENST00000590367.5:n.787-32C>A
ENST00000591382.5:c.1059-32C>A	ENSP00000467805.1:n.1059-32C>A
ENST00000591856.1:c.180-32C>A	ENSP00000468284.1:n.180-32C>A
ENST00000592576.5:c.1029-32C>A	ENSP00000465058.1:n.1029-32C>A
NM_001142605.1:c.954-32C>A	NP_001136077.1:n.954-32C>A
NM_001258353.1:c.1059-32C>A	NP_001245282.1:n.1059-32C>A
NM_001258354.1:c.1029-32C>A	NP_001245283.1:n.1029-32C>A
NM_004247.3:c.1059-32C>A	NP_004238.3:n.1059-32C>A
XR_934602.1:n.1144-32C>A
XR_934602.3:n.1140-32C>A
NM_004247.4:c.1059-32C>A MANE Select	NP_004238.3:n.1059-32C>A
NM_001142605.2:c.954-32C>A	NP_001136077.1:n.954-32C>A
NM_001258353.2:c.1059-32C>A	NP_001245282.1:n.1059-32C>A
NM_001258354.2:c.1029-32C>A	NP_001245283.1:n.1029-32C>A