Canonical Allele Identifier: CA1425882999

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138024G= , CM000665.2:g.184138024G=	GRCh38
NC_000003.11:g.183855812G= , CM000665.1:g.183855812G=	GRCh37
NC_000003.10:g.185338506G=	NCBI36
NG_015826.1:g.8003G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.656G=
ENST00000468748.7:n.616G=
ENST00000484154.2:n.1254G=
ENST00000491008.6:n.1381G=
ENST00000492226.2:n.630G=
ENST00000492773.6:c.365G=
ENST00000647636.1:c.633G=	ENSP00000497505.1:p.Arg211=
ENST00000647909.1:c.657G=	ENSP00000498164.1:p.Arg219=
ENST00000648145.1:c.401G=
ENST00000648189.1:c.383G=
ENST00000648256.1:c.582G=	ENSP00000497356.1:p.Arg194=
ENST00000648314.1:c.633G=	ENSP00000496920.1:p.Arg211=
ENST00000648599.1:c.633G=	ENSP00000497159.1:p.Arg211=
ENST00000648630.1:c.627G=	ENSP00000497887.1:p.Arg209=
ENST00000648682.1:c.633G=	ENSP00000498185.1:p.Arg211=
ENST00000648882.1:c.*459G=	ENSP00000497603.1:n.*459G=
ENST00000648890.1:c.633G=	ENSP00000497503.1:p.Arg211=
ENST00000648915.2:c.633G= MANE Select	ENSP00000497160.1:p.Arg211=
ENST00000649545.1:c.367G=
ENST00000649688.1:c.633G=	ENSP00000497097.1:p.Arg211=
ENST00000649814.1:n.682G=
ENST00000650270.1:c.500G=
ENST00000273783.7:c.633G=	ENSP00000273783.3:p.Arg211=
ENST00000432982.5:c.245+1349G=
ENST00000444495.1:c.633G=	ENSP00000409142.1:p.Arg211=
ENST00000468748.5:n.86G=
ENST00000481054.5:n.634G=
ENST00000491008.5:n.597G=
ENST00000491144.5:n.1073G=
ENST00000498831.1:n.588G=
NM_003907.2:c.633G=	NP_003898.2:p.Arg211=
XR_924208.1:n.1584G=
NM_003907.3:c.633G= MANE Select	NP_003898.2:p.Arg211=
XM_011513266.3:c.-269G=	XP_011511568.1:n.-269G=
XR_001740352.2:n.996G=
XR_001740353.2:n.996G=
XR_924208.2:n.996G=