Canonical Allele Identifier: CA437146401

Gene: EIF2B5

Linked Data

• gnomAD v4: 3-184136629-C-A
• MyVariant Identifiers: chr3:g.183854417C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136629C>A , CM000665.2:g.184136629C>A	GRCh38
NC_000003.11:g.183854417C>A , CM000665.1:g.183854417C>A	GRCh37
NC_000003.10:g.185337111C>A	NCBI36
NG_015826.1:g.6608C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.213C>A	ENSP00000414775.1:p.Ala71=
ENST00000465218.3:n.236C>A
ENST00000468748.7:n.196C>A
ENST00000471832.2:c.*207C>A	ENSP00000497786.1:n.*207C>A
ENST00000491008.6:n.78C>A
ENST00000492226.2:n.210C>A
ENST00000647636.1:c.213C>A	ENSP00000497505.1:p.Ala71=
ENST00000647909.1:c.213C>A	ENSP00000498164.1:p.Ala71=
ENST00000648256.1:c.162C>A	ENSP00000497356.1:p.Ala54=
ENST00000648314.1:c.213C>A	ENSP00000496920.1:p.Ala71=
ENST00000648599.1:c.213C>A	ENSP00000497159.1:p.Ala71=
ENST00000648630.1:c.207C>A	ENSP00000497887.1:p.Ala69=
ENST00000648682.1:c.213C>A	ENSP00000498185.1:p.Ala71=
ENST00000648882.1:c.*39C>A	ENSP00000497603.1:n.*39C>A
ENST00000648890.1:c.213C>A	ENSP00000497503.1:p.Ala71=
ENST00000648915.2:c.213C>A MANE Select	ENSP00000497160.1:p.Ala71=
ENST00000649688.1:c.213C>A	ENSP00000497097.1:p.Ala71=
ENST00000649814.1:n.262C>A
ENST00000650244.1:c.358C>A	ENSP00000497227.1:n.358C>A
ENST00000650270.1:c.80C>A
ENST00000273783.7:c.213C>A	ENSP00000273783.3:p.Ala71=
ENST00000432569.1:c.213C>A	ENSP00000414775.1:p.Ala71=
ENST00000432982.5:c.199C>A
ENST00000444495.1:c.213C>A	ENSP00000409142.1:p.Ala71=
ENST00000471832.1:n.144C>A
ENST00000481054.5:n.214C>A
ENST00000491144.5:n.561C>A
ENST00000498831.1:n.69C>A
NM_003907.2:c.213C>A	NP_003898.2:p.Ala71=
XR_924208.1:n.1164C>A
NM_003907.3:c.213C>A MANE Select	NP_003898.2:p.Ala71=
XM_011513266.3:c.-689C>A	XP_011511568.1:n.-689C>A
XR_001740352.2:n.576C>A
XR_001740353.2:n.576C>A
XR_924208.2:n.576C>A