Canonical Allele Identifier: CA1425882991

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138013A= , CM000665.2:g.184138013A=	GRCh38
NC_000003.11:g.183855801A= , CM000665.1:g.183855801A=	GRCh37
NC_000003.10:g.185338495A=	NCBI36
NG_015826.1:g.7992A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.645A=
ENST00000468748.7:n.605A=
ENST00000484154.2:n.1243A=
ENST00000491008.6:n.1370A=
ENST00000492226.2:n.619A=
ENST00000492773.6:c.354A=
ENST00000647636.1:c.622A=	ENSP00000497505.1:p.Thr208=
ENST00000647909.1:c.646A=	ENSP00000498164.1:p.Thr216=
ENST00000648145.1:c.390A=
ENST00000648189.1:c.372A=
ENST00000648256.1:c.571A=	ENSP00000497356.1:p.Thr191=
ENST00000648314.1:c.622A=	ENSP00000496920.1:p.Thr208=
ENST00000648599.1:c.622A=	ENSP00000497159.1:p.Thr208=
ENST00000648630.1:c.616A=	ENSP00000497887.1:p.Thr206=
ENST00000648682.1:c.622A=	ENSP00000498185.1:p.Thr208=
ENST00000648882.1:c.*448A=	ENSP00000497603.1:n.*448A=
ENST00000648890.1:c.622A=	ENSP00000497503.1:p.Thr208=
ENST00000648915.2:c.622A= MANE Select	ENSP00000497160.1:p.Thr208=
ENST00000649545.1:c.356A=
ENST00000649688.1:c.622A=	ENSP00000497097.1:p.Thr208=
ENST00000649814.1:n.671A=
ENST00000650270.1:c.489A=
ENST00000273783.7:c.622A=	ENSP00000273783.3:p.Thr208=
ENST00000432982.5:c.245+1338A=
ENST00000444495.1:c.622A=	ENSP00000409142.1:p.Thr208=
ENST00000468748.5:n.75A=
ENST00000481054.5:n.623A=
ENST00000491008.5:n.586A=
ENST00000491144.5:n.1062A=
ENST00000498831.1:n.577A=
NM_003907.2:c.622A=	NP_003898.2:p.Thr208=
XR_924208.1:n.1573A=
NM_003907.3:c.622A= MANE Select	NP_003898.2:p.Thr208=
XM_011513266.3:c.-280A=	XP_011511568.1:n.-280A=
XR_001740352.2:n.985A=
XR_001740353.2:n.985A=
XR_924208.2:n.985A=