Canonical Allele Identifier: CA1425882301

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137546G= , CM000665.2:g.184137546G=	GRCh38
NC_000003.11:g.183855334G= , CM000665.1:g.183855334G=	GRCh37
NC_000003.10:g.185338028G=	NCBI36
NG_015826.1:g.7525G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000465218.3:n.344-74G=
ENST00000468748.7:n.304-74G=
ENST00000484154.2:n.868G=
ENST00000491008.6:n.995G=
ENST00000492226.2:n.318-74G=
ENST00000492773.6:c.53-74G=
ENST00000647636.1:c.321-74G=	ENSP00000497505.1:n.321-74G=
ENST00000647909.1:c.321-74G=	ENSP00000498164.1:n.321-74G=
ENST00000648145.1:c.89-74G=
ENST00000648189.1:c.71-74G=
ENST00000648256.1:c.270-74G=	ENSP00000497356.1:n.270-74G=
ENST00000648314.1:c.321-74G=	ENSP00000496920.1:n.321-74G=
ENST00000648599.1:c.321-74G=	ENSP00000497159.1:n.321-74G=
ENST00000648630.1:c.315-74G=	ENSP00000497887.1:n.315-74G=
ENST00000648682.1:c.321-74G=	ENSP00000498185.1:n.321-74G=
ENST00000648882.1:c.*147-74G=	ENSP00000497603.1:n.*147-74G=
ENST00000648890.1:c.321-74G=	ENSP00000497503.1:n.321-74G=
ENST00000648915.2:c.321-74G= MANE Select	ENSP00000497160.1:n.321-74G=
ENST00000649545.1:c.55-74G=
ENST00000649688.1:c.321-74G=	ENSP00000497097.1:n.321-74G=
ENST00000649814.1:n.370-74G=
ENST00000650244.1:c.466-74G=	ENSP00000497227.1:n.466-74G=
ENST00000650270.1:c.188-74G=
ENST00000273783.7:c.321-74G=	ENSP00000273783.3:n.321-74G=
ENST00000432982.5:c.245+871G=
ENST00000444495.1:c.321-74G=	ENSP00000409142.1:n.321-74G=
ENST00000481054.5:n.322-74G=
ENST00000491008.5:n.211G=
ENST00000491144.5:n.669-74G=
ENST00000498831.1:n.275+16G=
NM_003907.2:c.321-74G=	NP_003898.2:n.321-74G=
XR_924208.1:n.1272-74G=
NM_003907.3:c.321-74G= MANE Select	NP_003898.2:n.321-74G=
XM_011513266.3:c.-581-74G=	XP_011511568.1:n.-581-74G=
XR_001740352.2:n.684-74G=
XR_001740353.2:n.684-74G=
XR_924208.2:n.684-74G=