Canonical Allele Identifier: CA355382890

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855972A>T (hg19) ; chr3:g.184138184A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138184A>T , CM000665.2:g.184138184A>T	GRCh38
NC_000003.11:g.183855972A>T , CM000665.1:g.183855972A>T	GRCh37
NC_000003.10:g.185338666A>T	NCBI36
NG_015826.1:g.8163A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.726A>T
ENST00000468748.7:n.686A>T
ENST00000484154.2:n.1324A>T
ENST00000491008.6:n.1451A>T
ENST00000492226.2:n.700A>T
ENST00000492773.6:c.457A>T
ENST00000647636.1:c.703A>T	ENSP00000497505.1:p.Ser235Cys
ENST00000647909.1:c.727A>T	ENSP00000498164.1:p.Ser243Cys
ENST00000648145.1:c.471A>T
ENST00000648189.1:c.453A>T
ENST00000648256.1:c.652A>T	ENSP00000497356.1:p.Ser218Cys
ENST00000648314.1:c.703A>T	ENSP00000496920.1:p.Ser235Cys
ENST00000648599.1:c.703A>T	ENSP00000497159.1:p.Ser235Cys
ENST00000648630.1:c.697A>T	ENSP00000497887.1:p.Ser233Cys
ENST00000648682.1:c.703A>T	ENSP00000498185.1:p.Ser235Cys
ENST00000648882.1:c.*529A>T	ENSP00000497603.1:n.*529A>T
ENST00000648890.1:c.703A>T	ENSP00000497503.1:p.Ser235Cys
ENST00000648915.2:c.703A>T MANE Select	ENSP00000497160.1:p.Ser235Cys
ENST00000649545.1:c.437A>T
ENST00000649688.1:c.703A>T	ENSP00000497097.1:p.Ser235Cys
ENST00000649814.1:n.752A>T
ENST00000650270.1:c.570A>T
ENST00000273783.7:c.703A>T	ENSP00000273783.3:p.Ser235Cys
ENST00000432982.5:c.245+1509A>T
ENST00000444495.1:c.703A>T	ENSP00000409142.1:p.Ser235Cys
ENST00000468748.5:n.156A>T
ENST00000479833.1:n.19A>T
ENST00000481054.5:n.704A>T
ENST00000491008.5:n.667A>T
ENST00000491144.5:n.1143A>T
NM_003907.2:c.703A>T	NP_003898.2:p.Ser235Cys
XR_924208.1:n.1654A>T
NM_003907.3:c.703A>T MANE Select	NP_003898.2:p.Ser235Cys
XM_011513266.3:c.-199A>T	XP_011511568.1:n.-199A>T
XR_001740352.2:n.1066A>T
XR_001740353.2:n.1066A>T
XR_924208.2:n.1066A>T