Canonical Allele Identifier: CA399811705
Gene: EFTUD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44859903A>C , CM000679.2:g.44859903A>C GRCh38
NC_000017.10:g.42937271A>C , CM000679.1:g.42937271A>C GRCh37
NC_000017.9:g.40292797A>C NCBI36
NG_032674.1:g.44723T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000426333.7:c.1860+2T>G MANE Select ENSP00000392094.1:n.1860+2T>G
ENST00000402521.7:c.1755+2T>G ENSP00000385873.2:n.1755+2T>G
ENST00000426333.6:c.1860+2T>G ENSP00000392094.1:n.1860+2T>G
ENST00000586276.5:n.1522+2T>G
ENST00000590367.5:n.1588+2T>G
ENST00000591382.5:c.1860+2T>G ENSP00000467805.1:n.1860+2T>G
ENST00000592576.5:c.1830+2T>G ENSP00000465058.1:n.1830+2T>G
NM_001142605.1:c.1755+2T>G NP_001136077.1:n.1755+2T>G
NM_001258353.1:c.1860+2T>G NP_001245282.1:n.1860+2T>G
NM_001258354.1:c.1830+2T>G NP_001245283.1:n.1830+2T>G
NM_004247.3:c.1860+2T>G NP_004238.3:n.1860+2T>G
XR_934602.1:n.1945+2T>G
XR_934602.3:n.1941+2T>G
NM_004247.4:c.1860+2T>G MANE Select NP_004238.3:n.1860+2T>G
NM_001142605.2:c.1755+2T>G NP_001136077.1:n.1755+2T>G
NM_001258353.2:c.1860+2T>G NP_001245282.1:n.1860+2T>G
NM_001258354.2:c.1830+2T>G NP_001245283.1:n.1830+2T>G