Canonical Allele Identifier: CA1425880262

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184135560A= , CM000665.2:g.184135560A=	GRCh38
NC_000003.11:g.183853348A= , CM000665.1:g.183853348A=	GRCh37
NC_000003.10:g.185336042A=	NCBI36
NG_015826.1:g.5539A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000432569.2:c.175A=	ENSP00000414775.1:p.Ile59=
ENST00000465218.3:n.198A=
ENST00000468748.7:n.158A=
ENST00000471832.2:c.175A=	ENSP00000497786.1:p.Ile59=
ENST00000491008.6:n.40A=
ENST00000492226.2:n.172A=
ENST00000647636.1:c.175A=	ENSP00000497505.1:p.Ile59=
ENST00000647909.1:c.175A=	ENSP00000498164.1:p.Ile59=
ENST00000648256.1:c.124A=	ENSP00000497356.1:p.Ile42=
ENST00000648314.1:c.175A=	ENSP00000496920.1:p.Ile59=
ENST00000648599.1:c.175A=	ENSP00000497159.1:p.Ile59=
ENST00000648630.1:c.169A=	ENSP00000497887.1:p.Ile57=
ENST00000648682.1:c.175A=	ENSP00000498185.1:p.Ile59=
ENST00000648882.1:c.175A=	ENSP00000497603.1:p.Ile59=
ENST00000648890.1:c.175A=	ENSP00000497503.1:p.Ile59=
ENST00000648915.2:c.175A= MANE Select	ENSP00000497160.1:p.Ile59=
ENST00000649688.1:c.175A=	ENSP00000497097.1:p.Ile59=
ENST00000649814.1:n.224A=
ENST00000650244.1:c.67A=	ENSP00000497227.1:p.Ile23=
ENST00000650270.1:c.42A=
ENST00000273783.7:c.175A=	ENSP00000273783.3:p.Ile59=
ENST00000432569.1:c.175A=	ENSP00000414775.1:p.Ile59=
ENST00000432982.5:c.161A=
ENST00000444495.1:c.175A=	ENSP00000409142.1:p.Ile59=
ENST00000481054.5:n.176A=
ENST00000491144.5:n.523A=
NM_003907.2:c.175A=	NP_003898.2:p.Ile59=
XR_924208.1:n.1126A=
NM_003907.3:c.175A= MANE Select	NP_003898.2:p.Ile59=
XM_011513266.3:c.-727A=	XP_011511568.1:n.-727A=
XR_001740352.2:n.538A=
XR_001740353.2:n.538A=
XR_924208.2:n.538A=