Canonical Allele Identifier: CA355381531

Gene: EIF2B5

Linked Data

• MyVariant Identifiers: chr3:g.183854448T>G (hg19) ; chr3:g.184136660T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136660T>G , CM000665.2:g.184136660T>G	GRCh38
NC_000003.11:g.183854448T>G , CM000665.1:g.183854448T>G	GRCh37
NC_000003.10:g.185337142T>G	NCBI36
NG_015826.1:g.6639T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000432569.2:c.244T>G	ENSP00000414775.1:p.Phe82Val
ENST00000465218.3:n.267T>G
ENST00000468748.7:n.227T>G
ENST00000471832.2:c.*238T>G	ENSP00000497786.1:n.*238T>G
ENST00000491008.6:n.109T>G
ENST00000492226.2:n.241T>G
ENST00000647636.1:c.244T>G	ENSP00000497505.1:p.Phe82Val
ENST00000647909.1:c.244T>G	ENSP00000498164.1:p.Phe82Val
ENST00000648145.1:c.12T>G
ENST00000648256.1:c.193T>G	ENSP00000497356.1:p.Phe65Val
ENST00000648314.1:c.244T>G	ENSP00000496920.1:p.Phe82Val
ENST00000648599.1:c.244T>G	ENSP00000497159.1:p.Phe82Val
ENST00000648630.1:c.238T>G	ENSP00000497887.1:p.Phe80Val
ENST00000648682.1:c.244T>G	ENSP00000498185.1:p.Phe82Val
ENST00000648882.1:c.*70T>G	ENSP00000497603.1:n.*70T>G
ENST00000648890.1:c.244T>G	ENSP00000497503.1:p.Phe82Val
ENST00000648915.2:c.244T>G MANE Select	ENSP00000497160.1:p.Phe82Val
ENST00000649688.1:c.244T>G	ENSP00000497097.1:p.Phe82Val
ENST00000649814.1:n.293T>G
ENST00000650244.1:c.389T>G	ENSP00000497227.1:n.389T>G
ENST00000650270.1:c.111T>G
ENST00000273783.7:c.244T>G	ENSP00000273783.3:p.Phe82Val
ENST00000432569.1:c.244T>G	ENSP00000414775.1:p.Phe82Val
ENST00000432982.5:c.230T>G
ENST00000444495.1:c.244T>G	ENSP00000409142.1:p.Phe82Val
ENST00000471832.1:n.175T>G
ENST00000481054.5:n.245T>G
ENST00000491144.5:n.592T>G
ENST00000498831.1:n.100T>G
NM_003907.2:c.244T>G	NP_003898.2:p.Phe82Val
XR_924208.1:n.1195T>G
NM_003907.3:c.244T>G MANE Select	NP_003898.2:p.Phe82Val
XM_011513266.3:c.-658T>G	XP_011511568.1:n.-658T>G
XR_001740352.2:n.607T>G
XR_001740353.2:n.607T>G
XR_924208.2:n.607T>G