Canonical Allele Identifier: CA1425887145

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184141983A= , CM000665.2:g.184141983A=	GRCh38
NC_000003.11:g.183859771A= , CM000665.1:g.183859771A=	GRCh37
NC_000003.10:g.185342465A=	NCBI36
NG_015826.1:g.11962A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.1238A=
ENST00000468748.7:n.1458A=
ENST00000484154.2:n.1445A=
ENST00000491008.6:n.1963A=
ENST00000492226.2:n.1482A=
ENST00000492773.6:c.969A=
ENST00000647636.1:c.*64A=	ENSP00000497505.1:n.*64A=
ENST00000647909.1:c.1239A=	ENSP00000498164.1:p.Gly413=
ENST00000648145.1:c.987A=
ENST00000648189.1:c.1033A=
ENST00000648256.1:c.1187A=	ENSP00000497356.1:n.1187A=
ENST00000648314.1:c.*334A=	ENSP00000496920.1:n.*334A=
ENST00000648599.1:c.*498A=	ENSP00000497159.1:n.*498A=
ENST00000648630.1:c.1094A=	ENSP00000497887.1:p.Glu365=
ENST00000648682.1:c.*55A=	ENSP00000498185.1:n.*55A=
ENST00000648882.1:c.*1041A=	ENSP00000497603.1:n.*1041A=
ENST00000648890.1:c.1215A=	ENSP00000497503.1:p.Gly405=
ENST00000648915.2:c.1215A= MANE Select	ENSP00000497160.1:p.Gly405=
ENST00000649545.1:c.636A=
ENST00000649688.1:c.*508A=	ENSP00000497097.1:n.*508A=
ENST00000649814.1:n.1264A=
ENST00000650270.1:c.1082A=
ENST00000273783.7:c.1215A=	ENSP00000273783.3:p.Gly405=
ENST00000432982.5:c.246-254A=
ENST00000444495.1:c.1215A=	ENSP00000409142.1:p.Gly405=
ENST00000479833.1:n.416A=
ENST00000481054.5:n.1309A=
ENST00000491144.5:n.1719A=
ENST00000492773.5:n.98A=
NM_003907.2:c.1215A=	NP_003898.2:p.Gly405=
XM_011513265.1:c.465A=	XP_011511567.1:p.Gly155=
XM_011513266.1:c.378A=	XP_011511568.1:p.Gly126=
XR_924208.1:n.2166A=
NM_003907.3:c.1215A= MANE Select	NP_003898.2:p.Gly405=
XM_011513266.3:c.378A=	XP_011511568.1:p.Gly126=
XR_001740352.2:n.1578A=
XR_001740353.2:n.1578A=
XR_924208.2:n.1578A=