Canonical Allele Identifier: CA2261586546
Gene: EFTUD2 HGNC NCBI

Linked Data

dbSNP Id: rs917129609

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44855010C>A , CM000679.2:g.44855010C>A GRCh38
NC_000017.10:g.42932378C>A , CM000679.1:g.42932378C>A GRCh37
NC_000017.9:g.40287904C>A NCBI36
NG_032674.1:g.49616G>T

Transcript Alleles

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