Canonical Allele Identifier: CA2638259533

Gene: EFTUD2

Linked Data

• gnomAD v4: 17-44855025-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.44855025T>G , CM000679.2:g.44855025T>G	GRCh38
NC_000017.10:g.42932393T>G , CM000679.1:g.42932393T>G	GRCh37
NC_000017.9:g.40287919T>G	NCBI36
NG_032674.1:g.49601A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426333.7:c.2046-21A>C MANE Select	ENSP00000392094.1:n.2046-21A>C
ENST00000402521.7:c.1941-21A>C	ENSP00000385873.2:n.1941-21A>C
ENST00000426333.6:c.2046-21A>C	ENSP00000392094.1:n.2046-21A>C
ENST00000586276.5:n.1708-21A>C
ENST00000588340.1:n.566-21A>C
ENST00000590124.5:c.48-21A>C	ENSP00000467249.1:n.48-21A>C
ENST00000590367.5:n.1774-21A>C
ENST00000590977.5:n.654-21A>C
ENST00000591382.5:c.2046-21A>C	ENSP00000467805.1:n.2046-21A>C
ENST00000592576.5:c.2016-21A>C	ENSP00000465058.1:n.2016-21A>C
NM_001142605.1:c.1941-21A>C	NP_001136077.1:n.1941-21A>C
NM_001258353.1:c.2046-21A>C	NP_001245282.1:n.2046-21A>C
NM_001258354.1:c.2016-21A>C	NP_001245283.1:n.2016-21A>C
NM_004247.3:c.2046-21A>C	NP_004238.3:n.2046-21A>C
XR_934602.1:n.2131-21A>C
XR_934602.3:n.2127-21A>C
NM_004247.4:c.2046-21A>C MANE Select	NP_004238.3:n.2046-21A>C
NM_001142605.2:c.1941-21A>C	NP_001136077.1:n.1941-21A>C
NM_001258353.2:c.2046-21A>C	NP_001245282.1:n.2046-21A>C
NM_001258354.2:c.2016-21A>C	NP_001245283.1:n.2016-21A>C