Canonical Allele Identifier: CA1425883033

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138056G= , CM000665.2:g.184138056G=	GRCh38
NC_000003.11:g.183855844G= , CM000665.1:g.183855844G=	GRCh37
NC_000003.10:g.185338538G=	NCBI36
NG_015826.1:g.8035G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.688G=
ENST00000468748.7:n.648G=
ENST00000484154.2:n.1286G=
ENST00000491008.6:n.1413G=
ENST00000492226.2:n.662G=
ENST00000492773.6:c.397G=
ENST00000647636.1:c.665G=	ENSP00000497505.1:p.Arg222=
ENST00000647909.1:c.689G=	ENSP00000498164.1:p.Arg230=
ENST00000648145.1:c.433G=
ENST00000648189.1:c.415G=
ENST00000648256.1:c.614G=	ENSP00000497356.1:p.Arg205=
ENST00000648314.1:c.665G=	ENSP00000496920.1:p.Arg222=
ENST00000648599.1:c.665G=	ENSP00000497159.1:p.Arg222=
ENST00000648630.1:c.659G=	ENSP00000497887.1:p.Arg220=
ENST00000648682.1:c.665G=	ENSP00000498185.1:p.Arg222=
ENST00000648882.1:c.*491G=	ENSP00000497603.1:n.*491G=
ENST00000648890.1:c.665G=	ENSP00000497503.1:p.Arg222=
ENST00000648915.2:c.665G= MANE Select	ENSP00000497160.1:p.Arg222=
ENST00000649545.1:c.399G=
ENST00000649688.1:c.665G=	ENSP00000497097.1:p.Arg222=
ENST00000649814.1:n.714G=
ENST00000650270.1:c.532G=
ENST00000273783.7:c.665G=	ENSP00000273783.3:p.Arg222=
ENST00000432982.5:c.245+1381G=
ENST00000444495.1:c.665G=	ENSP00000409142.1:p.Arg222=
ENST00000468748.5:n.118G=
ENST00000481054.5:n.666G=
ENST00000491008.5:n.629G=
ENST00000491144.5:n.1105G=
NM_003907.2:c.665G=	NP_003898.2:p.Arg222=
XR_924208.1:n.1616G=
NM_003907.3:c.665G= MANE Select	NP_003898.2:p.Arg222=
XM_011513266.3:c.-237G=	XP_011511568.1:n.-237G=
XR_001740352.2:n.1028G=
XR_001740353.2:n.1028G=
XR_924208.2:n.1028G=