Canonical Allele Identifier: CA355381363

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183853342T>G (hg19) ; chr3:g.184135554T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184135554T>G , CM000665.2:g.184135554T>G	GRCh38
NC_000003.11:g.183853342T>G , CM000665.1:g.183853342T>G	GRCh37
NC_000003.10:g.185336036T>G	NCBI36
NG_015826.1:g.5533T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000432569.2:c.169T>G	ENSP00000414775.1:p.Phe57Val
ENST00000465218.3:n.192T>G
ENST00000468748.7:n.152T>G
ENST00000471832.2:c.169T>G	ENSP00000497786.1:p.Phe57Val
ENST00000491008.6:n.34T>G
ENST00000492226.2:n.166T>G
ENST00000647636.1:c.169T>G	ENSP00000497505.1:p.Phe57Val
ENST00000647909.1:c.169T>G	ENSP00000498164.1:p.Phe57Val
ENST00000648256.1:c.118T>G	ENSP00000497356.1:p.Phe40Val
ENST00000648314.1:c.169T>G	ENSP00000496920.1:p.Phe57Val
ENST00000648599.1:c.169T>G	ENSP00000497159.1:p.Phe57Val
ENST00000648630.1:c.163T>G	ENSP00000497887.1:p.Phe55Val
ENST00000648682.1:c.169T>G	ENSP00000498185.1:p.Phe57Val
ENST00000648882.1:c.169T>G	ENSP00000497603.1:p.Phe57Val
ENST00000648890.1:c.169T>G	ENSP00000497503.1:p.Phe57Val
ENST00000648915.2:c.169T>G MANE Select	ENSP00000497160.1:p.Phe57Val
ENST00000649688.1:c.169T>G	ENSP00000497097.1:p.Phe57Val
ENST00000649814.1:n.218T>G
ENST00000650244.1:c.61T>G	ENSP00000497227.1:p.Phe21Val
ENST00000650270.1:c.36T>G
ENST00000273783.7:c.169T>G	ENSP00000273783.3:p.Phe57Val
ENST00000432569.1:c.169T>G	ENSP00000414775.1:p.Phe57Val
ENST00000432982.5:c.155T>G
ENST00000444495.1:c.169T>G	ENSP00000409142.1:p.Phe57Val
ENST00000481054.5:n.170T>G
ENST00000491144.5:n.517T>G
NM_003907.2:c.169T>G	NP_003898.2:p.Phe57Val
XR_924208.1:n.1120T>G
NM_003907.3:c.169T>G MANE Select	NP_003898.2:p.Phe57Val
XM_011513266.3:c.-733T>G	XP_011511568.1:n.-733T>G
XR_001740352.2:n.532T>G
XR_001740353.2:n.532T>G
XR_924208.2:n.532T>G