Canonical Allele Identifier: CA355381525

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183854446A>C (hg19) ; chr3:g.184136658A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136658A>C , CM000665.2:g.184136658A>C	GRCh38
NC_000003.11:g.183854446A>C , CM000665.1:g.183854446A>C	GRCh37
NC_000003.10:g.185337140A>C	NCBI36
NG_015826.1:g.6637A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432569.2:c.242A>C	ENSP00000414775.1:p.Glu81Ala
ENST00000465218.3:n.265A>C
ENST00000468748.7:n.225A>C
ENST00000471832.2:c.*236A>C	ENSP00000497786.1:n.*236A>C
ENST00000491008.6:n.107A>C
ENST00000492226.2:n.239A>C
ENST00000647636.1:c.242A>C	ENSP00000497505.1:p.Glu81Ala
ENST00000647909.1:c.242A>C	ENSP00000498164.1:p.Glu81Ala
ENST00000648145.1:c.10A>C
ENST00000648256.1:c.191A>C	ENSP00000497356.1:p.Glu64Ala
ENST00000648314.1:c.242A>C	ENSP00000496920.1:p.Glu81Ala
ENST00000648599.1:c.242A>C	ENSP00000497159.1:p.Glu81Ala
ENST00000648630.1:c.236A>C	ENSP00000497887.1:p.Glu79Ala
ENST00000648682.1:c.242A>C	ENSP00000498185.1:p.Glu81Ala
ENST00000648882.1:c.*68A>C	ENSP00000497603.1:n.*68A>C
ENST00000648890.1:c.242A>C	ENSP00000497503.1:p.Glu81Ala
ENST00000648915.2:c.242A>C MANE Select	ENSP00000497160.1:p.Glu81Ala
ENST00000649688.1:c.242A>C	ENSP00000497097.1:p.Glu81Ala
ENST00000649814.1:n.291A>C
ENST00000650244.1:c.387A>C	ENSP00000497227.1:n.387A>C
ENST00000650270.1:c.109A>C
ENST00000273783.7:c.242A>C	ENSP00000273783.3:p.Glu81Ala
ENST00000432569.1:c.242A>C	ENSP00000414775.1:p.Glu81Ala
ENST00000432982.5:c.228A>C
ENST00000444495.1:c.242A>C	ENSP00000409142.1:p.Glu81Ala
ENST00000471832.1:n.173A>C
ENST00000481054.5:n.243A>C
ENST00000491144.5:n.590A>C
ENST00000498831.1:n.98A>C
NM_003907.2:c.242A>C	NP_003898.2:p.Glu81Ala
XR_924208.1:n.1193A>C
NM_003907.3:c.242A>C MANE Select	NP_003898.2:p.Glu81Ala
XM_011513266.3:c.-660A>C	XP_011511568.1:n.-660A>C
XR_001740352.2:n.605A>C
XR_001740353.2:n.605A>C
XR_924208.2:n.605A>C