Canonical Allele Identifier: CA355382285

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855762C>G (hg19) ; chr3:g.184137974C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137974C>G , CM000665.2:g.184137974C>G	GRCh38
NC_000003.11:g.183855762C>G , CM000665.1:g.183855762C>G	GRCh37
NC_000003.10:g.185338456C>G	NCBI36
NG_015826.1:g.7953C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.606C>G
ENST00000468748.7:n.566C>G
ENST00000484154.2:n.1204C>G
ENST00000491008.6:n.1331C>G
ENST00000492226.2:n.580C>G
ENST00000492773.6:c.315C>G
ENST00000647636.1:c.583C>G	ENSP00000497505.1:p.Arg195Gly
ENST00000647909.1:c.607C>G	ENSP00000498164.1:p.Arg203Gly
ENST00000648145.1:c.351C>G
ENST00000648189.1:c.333C>G
ENST00000648256.1:c.532C>G	ENSP00000497356.1:p.Arg178Gly
ENST00000648314.1:c.583C>G	ENSP00000496920.1:p.Arg195Gly
ENST00000648599.1:c.583C>G	ENSP00000497159.1:p.Arg195Gly
ENST00000648630.1:c.577C>G	ENSP00000497887.1:p.Arg193Gly
ENST00000648682.1:c.583C>G	ENSP00000498185.1:p.Arg195Gly
ENST00000648882.1:c.*409C>G	ENSP00000497603.1:n.*409C>G
ENST00000648890.1:c.583C>G	ENSP00000497503.1:p.Arg195Gly
ENST00000648915.2:c.583C>G MANE Select	ENSP00000497160.1:p.Arg195Gly
ENST00000649545.1:c.317C>G
ENST00000649688.1:c.583C>G	ENSP00000497097.1:p.Arg195Gly
ENST00000649814.1:n.632C>G
ENST00000650270.1:c.450C>G
ENST00000273783.7:c.583C>G	ENSP00000273783.3:p.Arg195Gly
ENST00000432982.5:c.245+1299C>G
ENST00000444495.1:c.583C>G	ENSP00000409142.1:p.Arg195Gly
ENST00000468748.5:n.36C>G
ENST00000481054.5:n.584C>G
ENST00000491008.5:n.547C>G
ENST00000491144.5:n.1023C>G
ENST00000498831.1:n.538C>G
NM_003907.2:c.583C>G	NP_003898.2:p.Arg195Gly
XR_924208.1:n.1534C>G
NM_003907.3:c.583C>G MANE Select	NP_003898.2:p.Arg195Gly
XM_011513266.3:c.-319C>G	XP_011511568.1:n.-319C>G
XR_001740352.2:n.946C>G
XR_001740353.2:n.946C>G
XR_924208.2:n.946C>G