Canonical Allele Identifier: CA2576293799

Gene: EFTUD2

Linked Data

• gnomAD v4: 17-44854885-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44854888dup , CM000679.2:g.44854888dup	GRCh38
NC_000017.10:g.42932256dup , CM000679.1:g.42932256dup	GRCh37
NC_000017.9:g.40287782dup	NCBI36
NG_032674.1:g.49740dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.2132+32dup MANE Select	ENSP00000392094.1:n.2132+32dup
ENST00000402521.7:c.2027+32dup	ENSP00000385873.2:n.2027+32dup
ENST00000426333.6:c.2132+32dup	ENSP00000392094.1:n.2132+32dup
ENST00000586276.5:n.1794+32dup
ENST00000590124.5:c.134+32dup	ENSP00000467249.1:n.134+32dup
ENST00000590367.5:n.1860+32dup
ENST00000590977.5:n.740+32dup
ENST00000591382.5:c.2132+32dup	ENSP00000467805.1:n.2132+32dup
ENST00000592576.5:c.2102+32dup	ENSP00000465058.1:n.2102+32dup
NM_001142605.1:c.2027+32dup	NP_001136077.1:n.2027+32dup
NM_001258353.1:c.2132+32dup	NP_001245282.1:n.2132+32dup
NM_001258354.1:c.2102+32dup	NP_001245283.1:n.2102+32dup
NM_004247.3:c.2132+32dup	NP_004238.3:n.2132+32dup
XR_934602.1:n.2217+32dup
XR_934602.3:n.2213+32dup
NM_004247.4:c.2132+32dup MANE Select	NP_004238.3:n.2132+32dup
NM_001142605.2:c.2027+32dup	NP_001136077.1:n.2027+32dup
NM_001258353.2:c.2132+32dup	NP_001245282.1:n.2132+32dup
NM_001258354.2:c.2102+32dup	NP_001245283.1:n.2102+32dup