Canonical Allele Identifier: CA1425882344

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137579A= , CM000665.2:g.184137579A=	GRCh38
NC_000003.11:g.183855367A= , CM000665.1:g.183855367A=	GRCh37
NC_000003.10:g.185338061A=	NCBI36
NG_015826.1:g.7558A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000465218.3:n.344-41A=
ENST00000468748.7:n.304-41A=
ENST00000484154.2:n.901A=
ENST00000491008.6:n.1028A=
ENST00000492226.2:n.318-41A=
ENST00000492773.6:c.53-41A=
ENST00000647636.1:c.321-41A=	ENSP00000497505.1:n.321-41A=
ENST00000647909.1:c.321-41A=	ENSP00000498164.1:n.321-41A=
ENST00000648145.1:c.89-41A=
ENST00000648189.1:c.71-41A=
ENST00000648256.1:c.270-41A=	ENSP00000497356.1:n.270-41A=
ENST00000648314.1:c.321-41A=	ENSP00000496920.1:n.321-41A=
ENST00000648599.1:c.321-41A=	ENSP00000497159.1:n.321-41A=
ENST00000648630.1:c.315-41A=	ENSP00000497887.1:n.315-41A=
ENST00000648682.1:c.321-41A=	ENSP00000498185.1:n.321-41A=
ENST00000648882.1:c.*147-41A=	ENSP00000497603.1:n.*147-41A=
ENST00000648890.1:c.321-41A=	ENSP00000497503.1:n.321-41A=
ENST00000648915.2:c.321-41A= MANE Select	ENSP00000497160.1:n.321-41A=
ENST00000649545.1:c.55-41A=
ENST00000649688.1:c.321-41A=	ENSP00000497097.1:n.321-41A=
ENST00000649814.1:n.370-41A=
ENST00000650244.1:c.466-41A=	ENSP00000497227.1:n.466-41A=
ENST00000650270.1:c.188-41A=
ENST00000273783.7:c.321-41A=	ENSP00000273783.3:n.321-41A=
ENST00000432982.5:c.245+904A=
ENST00000444495.1:c.321-41A=	ENSP00000409142.1:n.321-41A=
ENST00000481054.5:n.322-41A=
ENST00000491008.5:n.244A=
ENST00000491144.5:n.669-41A=
ENST00000498831.1:n.276-41A=
NM_003907.2:c.321-41A=	NP_003898.2:n.321-41A=
XR_924208.1:n.1272-41A=
NM_003907.3:c.321-41A= MANE Select	NP_003898.2:n.321-41A=
XM_011513266.3:c.-581-41A=	XP_011511568.1:n.-581-41A=
XR_001740352.2:n.684-41A=
XR_001740353.2:n.684-41A=
XR_924208.2:n.684-41A=