Canonical Allele Identifier: CA1425883043

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138063T= , CM000665.2:g.184138063T=	GRCh38
NC_000003.11:g.183855851T= , CM000665.1:g.183855851T=	GRCh37
NC_000003.10:g.185338545T=	NCBI36
NG_015826.1:g.8042T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.695T=
ENST00000468748.7:n.655T=
ENST00000484154.2:n.1293T=
ENST00000491008.6:n.1420T=
ENST00000492226.2:n.669T=
ENST00000492773.6:c.404T=
ENST00000647636.1:c.672T=	ENSP00000497505.1:p.Phe224=
ENST00000647909.1:c.696T=	ENSP00000498164.1:p.Phe232=
ENST00000648145.1:c.440T=
ENST00000648189.1:c.422T=
ENST00000648256.1:c.621T=	ENSP00000497356.1:p.Phe207=
ENST00000648314.1:c.672T=	ENSP00000496920.1:p.Phe224=
ENST00000648599.1:c.672T=	ENSP00000497159.1:p.Phe224=
ENST00000648630.1:c.666T=	ENSP00000497887.1:p.Phe222=
ENST00000648682.1:c.672T=	ENSP00000498185.1:p.Phe224=
ENST00000648882.1:c.*498T=	ENSP00000497603.1:n.*498T=
ENST00000648890.1:c.672T=	ENSP00000497503.1:p.Phe224=
ENST00000648915.2:c.672T= MANE Select	ENSP00000497160.1:p.Phe224=
ENST00000649545.1:c.406T=
ENST00000649688.1:c.672T=	ENSP00000497097.1:p.Phe224=
ENST00000649814.1:n.721T=
ENST00000650270.1:c.539T=
ENST00000273783.7:c.672T=	ENSP00000273783.3:p.Phe224=
ENST00000432982.5:c.245+1388T=
ENST00000444495.1:c.672T=	ENSP00000409142.1:p.Phe224=
ENST00000468748.5:n.125T=
ENST00000481054.5:n.673T=
ENST00000491008.5:n.636T=
ENST00000491144.5:n.1112T=
NM_003907.2:c.672T=	NP_003898.2:p.Phe224=
XR_924208.1:n.1623T=
NM_003907.3:c.672T= MANE Select	NP_003898.2:p.Phe224=
XM_011513266.3:c.-230T=	XP_011511568.1:n.-230T=
XR_001740352.2:n.1035T=
XR_001740353.2:n.1035T=
XR_924208.2:n.1035T=