Canonical Allele Identifier: CA355381528

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183854447A>C (hg19) ; chr3:g.184136659A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136659A>C , CM000665.2:g.184136659A>C	GRCh38
NC_000003.11:g.183854447A>C , CM000665.1:g.183854447A>C	GRCh37
NC_000003.10:g.185337141A>C	NCBI36
NG_015826.1:g.6638A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000432569.2:c.243A>C	ENSP00000414775.1:p.Glu81Asp
ENST00000465218.3:n.266A>C
ENST00000468748.7:n.226A>C
ENST00000471832.2:c.*237A>C	ENSP00000497786.1:n.*237A>C
ENST00000491008.6:n.108A>C
ENST00000492226.2:n.240A>C
ENST00000647636.1:c.243A>C	ENSP00000497505.1:p.Glu81Asp
ENST00000647909.1:c.243A>C	ENSP00000498164.1:p.Glu81Asp
ENST00000648145.1:c.11A>C
ENST00000648256.1:c.192A>C	ENSP00000497356.1:p.Glu64Asp
ENST00000648314.1:c.243A>C	ENSP00000496920.1:p.Glu81Asp
ENST00000648599.1:c.243A>C	ENSP00000497159.1:p.Glu81Asp
ENST00000648630.1:c.237A>C	ENSP00000497887.1:p.Glu79Asp
ENST00000648682.1:c.243A>C	ENSP00000498185.1:p.Glu81Asp
ENST00000648882.1:c.*69A>C	ENSP00000497603.1:n.*69A>C
ENST00000648890.1:c.243A>C	ENSP00000497503.1:p.Glu81Asp
ENST00000648915.2:c.243A>C MANE Select	ENSP00000497160.1:p.Glu81Asp
ENST00000649688.1:c.243A>C	ENSP00000497097.1:p.Glu81Asp
ENST00000649814.1:n.292A>C
ENST00000650244.1:c.388A>C	ENSP00000497227.1:n.388A>C
ENST00000650270.1:c.110A>C
ENST00000273783.7:c.243A>C	ENSP00000273783.3:p.Glu81Asp
ENST00000432569.1:c.243A>C	ENSP00000414775.1:p.Glu81Asp
ENST00000432982.5:c.229A>C
ENST00000444495.1:c.243A>C	ENSP00000409142.1:p.Glu81Asp
ENST00000471832.1:n.174A>C
ENST00000481054.5:n.244A>C
ENST00000491144.5:n.591A>C
ENST00000498831.1:n.99A>C
NM_003907.2:c.243A>C	NP_003898.2:p.Glu81Asp
XR_924208.1:n.1194A>C
NM_003907.3:c.243A>C MANE Select	NP_003898.2:p.Glu81Asp
XM_011513266.3:c.-659A>C	XP_011511568.1:n.-659A>C
XR_001740352.2:n.606A>C
XR_001740353.2:n.606A>C
XR_924208.2:n.606A>C