Canonical Allele Identifier: CA355382968

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855990C>G (hg19) ; chr3:g.184138202C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138202C>G , CM000665.2:g.184138202C>G	GRCh38
NC_000003.11:g.183855990C>G , CM000665.1:g.183855990C>G	GRCh37
NC_000003.10:g.185338684C>G	NCBI36
NG_015826.1:g.8181C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.744C>G
ENST00000468748.7:n.704C>G
ENST00000484154.2:n.1342C>G
ENST00000491008.6:n.1469C>G
ENST00000492226.2:n.718C>G
ENST00000492773.6:c.475C>G
ENST00000647636.1:c.721C>G	ENSP00000497505.1:p.Arg241Gly
ENST00000647909.1:c.745C>G	ENSP00000498164.1:p.Arg249Gly
ENST00000648145.1:c.489C>G
ENST00000648189.1:c.471C>G
ENST00000648256.1:c.670C>G	ENSP00000497356.1:p.Arg224Gly
ENST00000648314.1:c.721C>G	ENSP00000496920.1:p.Arg241Gly
ENST00000648599.1:c.721C>G	ENSP00000497159.1:p.Arg241Gly
ENST00000648630.1:c.715C>G	ENSP00000497887.1:p.Arg239Gly
ENST00000648682.1:c.721C>G	ENSP00000498185.1:p.Arg241Gly
ENST00000648882.1:c.*547C>G	ENSP00000497603.1:n.*547C>G
ENST00000648890.1:c.721C>G	ENSP00000497503.1:p.Arg241Gly
ENST00000648915.2:c.721C>G MANE Select	ENSP00000497160.1:p.Arg241Gly
ENST00000649545.1:c.455C>G
ENST00000649688.1:c.721C>G	ENSP00000497097.1:p.Arg241Gly
ENST00000649814.1:n.770C>G
ENST00000650270.1:c.588C>G
ENST00000273783.7:c.721C>G	ENSP00000273783.3:p.Arg241Gly
ENST00000432982.5:c.245+1527C>G
ENST00000444495.1:c.721C>G	ENSP00000409142.1:p.Arg241Gly
ENST00000468748.5:n.174C>G
ENST00000479833.1:n.37C>G
ENST00000481054.5:n.722C>G
ENST00000491008.5:n.685C>G
ENST00000491144.5:n.1161C>G
NM_003907.2:c.721C>G	NP_003898.2:p.Arg241Gly
XR_924208.1:n.1672C>G
NM_003907.3:c.721C>G MANE Select	NP_003898.2:p.Arg241Gly
XM_011513266.3:c.-181C>G	XP_011511568.1:n.-181C>G
XR_001740352.2:n.1084C>G
XR_001740353.2:n.1084C>G
XR_924208.2:n.1084C>G