Canonical Allele Identifier: CA355381578

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183854472G>C (hg19) ; chr3:g.184136684G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136684G>C , CM000665.2:g.184136684G>C	GRCh38
NC_000003.11:g.183854472G>C , CM000665.1:g.183854472G>C	GRCh37
NC_000003.10:g.185337166G>C	NCBI36
NG_015826.1:g.6663G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.268G>C	ENSP00000414775.1:p.Glu90Gln
ENST00000465218.3:n.291G>C
ENST00000468748.7:n.251G>C
ENST00000471832.2:c.*262G>C	ENSP00000497786.1:n.*262G>C
ENST00000484154.2:n.6G>C
ENST00000491008.6:n.133G>C
ENST00000492226.2:n.265G>C
ENST00000647636.1:c.268G>C	ENSP00000497505.1:p.Glu90Gln
ENST00000647909.1:c.268G>C	ENSP00000498164.1:p.Glu90Gln
ENST00000648145.1:c.36G>C
ENST00000648189.1:c.18G>C
ENST00000648256.1:c.217G>C	ENSP00000497356.1:p.Glu73Gln
ENST00000648314.1:c.268G>C	ENSP00000496920.1:p.Glu90Gln
ENST00000648599.1:c.268G>C	ENSP00000497159.1:p.Glu90Gln
ENST00000648630.1:c.262G>C	ENSP00000497887.1:p.Glu88Gln
ENST00000648682.1:c.268G>C	ENSP00000498185.1:p.Glu90Gln
ENST00000648882.1:c.*94G>C	ENSP00000497603.1:n.*94G>C
ENST00000648890.1:c.268G>C	ENSP00000497503.1:p.Glu90Gln
ENST00000648915.2:c.268G>C MANE Select	ENSP00000497160.1:p.Glu90Gln
ENST00000649545.1:c.2G>C
ENST00000649688.1:c.268G>C	ENSP00000497097.1:p.Glu90Gln
ENST00000649814.1:n.317G>C
ENST00000650244.1:c.413G>C	ENSP00000497227.1:n.413G>C
ENST00000650270.1:c.135G>C
ENST00000273783.7:c.268G>C	ENSP00000273783.3:p.Glu90Gln
ENST00000432569.1:c.268G>C	ENSP00000414775.1:p.Glu90Gln
ENST00000432982.5:c.245+9G>C
ENST00000444495.1:c.268G>C	ENSP00000409142.1:p.Glu90Gln
ENST00000471832.1:n.199G>C
ENST00000481054.5:n.269G>C
ENST00000491144.5:n.616G>C
ENST00000498831.1:n.124G>C
NM_003907.2:c.268G>C	NP_003898.2:p.Glu90Gln
XR_924208.1:n.1219G>C
NM_003907.3:c.268G>C MANE Select	NP_003898.2:p.Glu90Gln
XM_011513266.3:c.-634G>C	XP_011511568.1:n.-634G>C
XR_001740352.2:n.631G>C
XR_001740353.2:n.631G>C
XR_924208.2:n.631G>C