Canonical Allele Identifier: CA355381652

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183854503C>A (hg19) ; chr3:g.184136715C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136715C>A , CM000665.2:g.184136715C>A	GRCh38
NC_000003.11:g.183854503C>A , CM000665.1:g.183854503C>A	GRCh37
NC_000003.10:g.185337197C>A	NCBI36
NG_015826.1:g.6694C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.299C>A	ENSP00000414775.1:p.Ala100Asp
ENST00000465218.3:n.322C>A
ENST00000468748.7:n.282C>A
ENST00000471832.2:c.*293C>A	ENSP00000497786.1:n.*293C>A
ENST00000484154.2:n.37C>A
ENST00000491008.6:n.164C>A
ENST00000492226.2:n.296C>A
ENST00000492773.6:c.31C>A
ENST00000647636.1:c.299C>A	ENSP00000497505.1:p.Ala100Asp
ENST00000647909.1:c.299C>A	ENSP00000498164.1:p.Ala100Asp
ENST00000648145.1:c.67C>A
ENST00000648189.1:c.49C>A
ENST00000648256.1:c.248C>A	ENSP00000497356.1:p.Ala83Asp
ENST00000648314.1:c.299C>A	ENSP00000496920.1:p.Ala100Asp
ENST00000648599.1:c.299C>A	ENSP00000497159.1:p.Ala100Asp
ENST00000648630.1:c.293C>A	ENSP00000497887.1:p.Ala98Asp
ENST00000648682.1:c.299C>A	ENSP00000498185.1:p.Ala100Asp
ENST00000648882.1:c.*125C>A	ENSP00000497603.1:n.*125C>A
ENST00000648890.1:c.299C>A	ENSP00000497503.1:p.Ala100Asp
ENST00000648915.2:c.299C>A MANE Select	ENSP00000497160.1:p.Ala100Asp
ENST00000649545.1:c.33C>A
ENST00000649688.1:c.299C>A	ENSP00000497097.1:p.Ala100Asp
ENST00000649814.1:n.348C>A
ENST00000650244.1:c.444C>A	ENSP00000497227.1:n.444C>A
ENST00000650270.1:c.166C>A
ENST00000273783.7:c.299C>A	ENSP00000273783.3:p.Ala100Asp
ENST00000432569.1:c.299C>A	ENSP00000414775.1:p.Ala100Asp
ENST00000432982.5:c.245+40C>A
ENST00000444495.1:c.299C>A	ENSP00000409142.1:p.Ala100Asp
ENST00000471832.1:n.230C>A
ENST00000481054.5:n.300C>A
ENST00000491144.5:n.647C>A
ENST00000498831.1:n.155C>A
NM_003907.2:c.299C>A	NP_003898.2:p.Ala100Asp
XR_924208.1:n.1250C>A
NM_003907.3:c.299C>A MANE Select	NP_003898.2:p.Ala100Asp
XM_011513266.3:c.-603C>A	XP_011511568.1:n.-603C>A
XR_001740352.2:n.662C>A
XR_001740353.2:n.662C>A
XR_924208.2:n.662C>A