Canonical Allele Identifier: CA355382443

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855835A>G (hg19) ; chr3:g.184138047A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138047A>G , CM000665.2:g.184138047A>G	GRCh38
NC_000003.11:g.183855835A>G , CM000665.1:g.183855835A>G	GRCh37
NC_000003.10:g.185338529A>G	NCBI36
NG_015826.1:g.8026A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.679A>G
ENST00000468748.7:n.639A>G
ENST00000484154.2:n.1277A>G
ENST00000491008.6:n.1404A>G
ENST00000492226.2:n.653A>G
ENST00000492773.6:c.388A>G
ENST00000647636.1:c.656A>G	ENSP00000497505.1:p.Gln219Arg
ENST00000647909.1:c.680A>G	ENSP00000498164.1:p.Gln227Arg
ENST00000648145.1:c.424A>G
ENST00000648189.1:c.406A>G
ENST00000648256.1:c.605A>G	ENSP00000497356.1:p.Gln202Arg
ENST00000648314.1:c.656A>G	ENSP00000496920.1:p.Gln219Arg
ENST00000648599.1:c.656A>G	ENSP00000497159.1:p.Gln219Arg
ENST00000648630.1:c.650A>G	ENSP00000497887.1:p.Gln217Arg
ENST00000648682.1:c.656A>G	ENSP00000498185.1:p.Gln219Arg
ENST00000648882.1:c.*482A>G	ENSP00000497603.1:n.*482A>G
ENST00000648890.1:c.656A>G	ENSP00000497503.1:p.Gln219Arg
ENST00000648915.2:c.656A>G MANE Select	ENSP00000497160.1:p.Gln219Arg
ENST00000649545.1:c.390A>G
ENST00000649688.1:c.656A>G	ENSP00000497097.1:p.Gln219Arg
ENST00000649814.1:n.705A>G
ENST00000650270.1:c.523A>G
ENST00000273783.7:c.656A>G	ENSP00000273783.3:p.Gln219Arg
ENST00000432982.5:c.245+1372A>G
ENST00000444495.1:c.656A>G	ENSP00000409142.1:p.Gln219Arg
ENST00000468748.5:n.109A>G
ENST00000481054.5:n.657A>G
ENST00000491008.5:n.620A>G
ENST00000491144.5:n.1096A>G
NM_003907.2:c.656A>G	NP_003898.2:p.Gln219Arg
XR_924208.1:n.1607A>G
NM_003907.3:c.656A>G MANE Select	NP_003898.2:p.Gln219Arg
XM_011513266.3:c.-246A>G	XP_011511568.1:n.-246A>G
XR_001740352.2:n.1019A>G
XR_001740353.2:n.1019A>G
XR_924208.2:n.1019A>G