Canonical Allele Identifier: CA355381547

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183854455C>A (hg19) ; chr3:g.184136667C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136667C>A , CM000665.2:g.184136667C>A	GRCh38
NC_000003.11:g.183854455C>A , CM000665.1:g.183854455C>A	GRCh37
NC_000003.10:g.185337149C>A	NCBI36
NG_015826.1:g.6646C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000432569.2:c.251C>A	ENSP00000414775.1:p.Thr84Asn
ENST00000465218.3:n.274C>A
ENST00000468748.7:n.234C>A
ENST00000471832.2:c.*245C>A	ENSP00000497786.1:n.*245C>A
ENST00000491008.6:n.116C>A
ENST00000492226.2:n.248C>A
ENST00000647636.1:c.251C>A	ENSP00000497505.1:p.Thr84Asn
ENST00000647909.1:c.251C>A	ENSP00000498164.1:p.Thr84Asn
ENST00000648145.1:c.19C>A
ENST00000648189.1:c.1C>A
ENST00000648256.1:c.200C>A	ENSP00000497356.1:p.Thr67Asn
ENST00000648314.1:c.251C>A	ENSP00000496920.1:p.Thr84Asn
ENST00000648599.1:c.251C>A	ENSP00000497159.1:p.Thr84Asn
ENST00000648630.1:c.245C>A	ENSP00000497887.1:p.Thr82Asn
ENST00000648682.1:c.251C>A	ENSP00000498185.1:p.Thr84Asn
ENST00000648882.1:c.*77C>A	ENSP00000497603.1:n.*77C>A
ENST00000648890.1:c.251C>A	ENSP00000497503.1:p.Thr84Asn
ENST00000648915.2:c.251C>A MANE Select	ENSP00000497160.1:p.Thr84Asn
ENST00000649688.1:c.251C>A	ENSP00000497097.1:p.Thr84Asn
ENST00000649814.1:n.300C>A
ENST00000650244.1:c.396C>A	ENSP00000497227.1:n.396C>A
ENST00000650270.1:c.118C>A
ENST00000273783.7:c.251C>A	ENSP00000273783.3:p.Thr84Asn
ENST00000432569.1:c.251C>A	ENSP00000414775.1:p.Thr84Asn
ENST00000432982.5:c.237C>A
ENST00000444495.1:c.251C>A	ENSP00000409142.1:p.Thr84Asn
ENST00000471832.1:n.182C>A
ENST00000481054.5:n.252C>A
ENST00000491144.5:n.599C>A
ENST00000498831.1:n.107C>A
NM_003907.2:c.251C>A	NP_003898.2:p.Thr84Asn
XR_924208.1:n.1202C>A
NM_003907.3:c.251C>A MANE Select	NP_003898.2:p.Thr84Asn
XM_011513266.3:c.-651C>A	XP_011511568.1:n.-651C>A
XR_001740352.2:n.614C>A
XR_001740353.2:n.614C>A
XR_924208.2:n.614C>A