Canonical Allele Identifier: CA355381665

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183854509T>A (hg19) ; chr3:g.184136721T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136721T>A , CM000665.2:g.184136721T>A	GRCh38
NC_000003.11:g.183854509T>A , CM000665.1:g.183854509T>A	GRCh37
NC_000003.10:g.185337203T>A	NCBI36
NG_015826.1:g.6700T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.305T>A	ENSP00000414775.1:p.Ile102Asn
ENST00000465218.3:n.328T>A
ENST00000468748.7:n.288T>A
ENST00000471832.2:c.*299T>A	ENSP00000497786.1:n.*299T>A
ENST00000484154.2:n.43T>A
ENST00000491008.6:n.170T>A
ENST00000492226.2:n.302T>A
ENST00000492773.6:c.37T>A
ENST00000647636.1:c.305T>A	ENSP00000497505.1:p.Ile102Asn
ENST00000647909.1:c.305T>A	ENSP00000498164.1:p.Ile102Asn
ENST00000648145.1:c.73T>A
ENST00000648189.1:c.55T>A
ENST00000648256.1:c.254T>A	ENSP00000497356.1:p.Ile85Asn
ENST00000648314.1:c.305T>A	ENSP00000496920.1:p.Ile102Asn
ENST00000648599.1:c.305T>A	ENSP00000497159.1:p.Ile102Asn
ENST00000648630.1:c.299T>A	ENSP00000497887.1:p.Ile100Asn
ENST00000648682.1:c.305T>A	ENSP00000498185.1:p.Ile102Asn
ENST00000648882.1:c.*131T>A	ENSP00000497603.1:n.*131T>A
ENST00000648890.1:c.305T>A	ENSP00000497503.1:p.Ile102Asn
ENST00000648915.2:c.305T>A MANE Select	ENSP00000497160.1:p.Ile102Asn
ENST00000649545.1:c.39T>A
ENST00000649688.1:c.305T>A	ENSP00000497097.1:p.Ile102Asn
ENST00000649814.1:n.354T>A
ENST00000650244.1:c.450T>A	ENSP00000497227.1:n.450T>A
ENST00000650270.1:c.172T>A
ENST00000273783.7:c.305T>A	ENSP00000273783.3:p.Ile102Asn
ENST00000432569.1:c.305T>A	ENSP00000414775.1:p.Ile102Asn
ENST00000432982.5:c.245+46T>A
ENST00000444495.1:c.305T>A	ENSP00000409142.1:p.Ile102Asn
ENST00000471832.1:n.236T>A
ENST00000481054.5:n.306T>A
ENST00000491144.5:n.653T>A
ENST00000498831.1:n.161T>A
NM_003907.2:c.305T>A	NP_003898.2:p.Ile102Asn
XR_924208.1:n.1256T>A
NM_003907.3:c.305T>A MANE Select	NP_003898.2:p.Ile102Asn
XM_011513266.3:c.-597T>A	XP_011511568.1:n.-597T>A
XR_001740352.2:n.668T>A
XR_001740353.2:n.668T>A
XR_924208.2:n.668T>A