Canonical Allele Identifier: CA355382080

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183855584A>C (hg19) ; chr3:g.184137796A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137796A>C , CM000665.2:g.184137796A>C	GRCh38
NC_000003.11:g.183855584A>C , CM000665.1:g.183855584A>C	GRCh37
NC_000003.10:g.185338278A>C	NCBI36
NG_015826.1:g.7775A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.520A>C
ENST00000468748.7:n.480A>C
ENST00000484154.2:n.1118A>C
ENST00000491008.6:n.1245A>C
ENST00000492226.2:n.494A>C
ENST00000492773.6:c.229A>C
ENST00000647636.1:c.497A>C	ENSP00000497505.1:p.Glu166Ala
ENST00000647909.1:c.497A>C	ENSP00000498164.1:p.Glu166Ala
ENST00000648145.1:c.265A>C
ENST00000648189.1:c.247A>C
ENST00000648256.1:c.446A>C	ENSP00000497356.1:p.Glu149Ala
ENST00000648314.1:c.497A>C	ENSP00000496920.1:p.Glu166Ala
ENST00000648599.1:c.497A>C	ENSP00000497159.1:p.Glu166Ala
ENST00000648630.1:c.491A>C	ENSP00000497887.1:p.Glu164Ala
ENST00000648682.1:c.497A>C	ENSP00000498185.1:p.Glu166Ala
ENST00000648882.1:c.*323A>C	ENSP00000497603.1:n.*323A>C
ENST00000648890.1:c.497A>C	ENSP00000497503.1:p.Glu166Ala
ENST00000648915.2:c.497A>C MANE Select	ENSP00000497160.1:p.Glu166Ala
ENST00000649545.1:c.231A>C
ENST00000649688.1:c.497A>C	ENSP00000497097.1:p.Glu166Ala
ENST00000649814.1:n.546A>C
ENST00000650244.1:c.642A>C	ENSP00000497227.1:n.642A>C
ENST00000650270.1:c.364A>C
ENST00000273783.7:c.497A>C	ENSP00000273783.3:p.Glu166Ala
ENST00000432982.5:c.245+1121A>C
ENST00000444495.1:c.497A>C	ENSP00000409142.1:p.Glu166Ala
ENST00000481054.5:n.498A>C
ENST00000491008.5:n.461A>C
ENST00000491144.5:n.845A>C
ENST00000498831.1:n.452A>C
NM_003907.2:c.497A>C	NP_003898.2:p.Glu166Ala
XR_924208.1:n.1448A>C
NM_003907.3:c.497A>C MANE Select	NP_003898.2:p.Glu166Ala
XM_011513266.3:c.-405A>C	XP_011511568.1:n.-405A>C
XR_001740352.2:n.860A>C
XR_001740353.2:n.860A>C
XR_924208.2:n.860A>C