Canonical Allele Identifier: CA355381553

Gene: EIF2B5

Linked Data

• dbSNP Id: rs1713374594
• MyVariant Identifiers: chr3:g.183854458C>T (hg19) ; chr3:g.184136670C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136670C>T , CM000665.2:g.184136670C>T	GRCh38
NC_000003.11:g.183854458C>T , CM000665.1:g.183854458C>T	GRCh37
NC_000003.10:g.185337152C>T	NCBI36
NG_015826.1:g.6649C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000432569.2:c.254C>T	ENSP00000414775.1:p.Ala85Val
ENST00000465218.3:n.277C>T
ENST00000468748.7:n.237C>T
ENST00000471832.2:c.*248C>T	ENSP00000497786.1:n.*248C>T
ENST00000491008.6:n.119C>T
ENST00000492226.2:n.251C>T
ENST00000647636.1:c.254C>T	ENSP00000497505.1:p.Ala85Val
ENST00000647909.1:c.254C>T	ENSP00000498164.1:p.Ala85Val
ENST00000648145.1:c.22C>T
ENST00000648189.1:c.4C>T
ENST00000648256.1:c.203C>T	ENSP00000497356.1:p.Ala68Val
ENST00000648314.1:c.254C>T	ENSP00000496920.1:p.Ala85Val
ENST00000648599.1:c.254C>T	ENSP00000497159.1:p.Ala85Val
ENST00000648630.1:c.248C>T	ENSP00000497887.1:p.Ala83Val
ENST00000648682.1:c.254C>T	ENSP00000498185.1:p.Ala85Val
ENST00000648882.1:c.*80C>T	ENSP00000497603.1:n.*80C>T
ENST00000648890.1:c.254C>T	ENSP00000497503.1:p.Ala85Val
ENST00000648915.2:c.254C>T MANE Select	ENSP00000497160.1:p.Ala85Val
ENST00000649688.1:c.254C>T	ENSP00000497097.1:p.Ala85Val
ENST00000649814.1:n.303C>T
ENST00000650244.1:c.399C>T	ENSP00000497227.1:n.399C>T
ENST00000650270.1:c.121C>T
ENST00000273783.7:c.254C>T	ENSP00000273783.3:p.Ala85Val
ENST00000432569.1:c.254C>T	ENSP00000414775.1:p.Ala85Val
ENST00000432982.5:c.240C>T
ENST00000444495.1:c.254C>T	ENSP00000409142.1:p.Ala85Val
ENST00000471832.1:n.185C>T
ENST00000481054.5:n.255C>T
ENST00000491144.5:n.602C>T
ENST00000498831.1:n.110C>T
NM_003907.2:c.254C>T	NP_003898.2:p.Ala85Val
XR_924208.1:n.1205C>T
NM_003907.3:c.254C>T MANE Select	NP_003898.2:p.Ala85Val
XM_011513266.3:c.-648C>T	XP_011511568.1:n.-648C>T
XR_001740352.2:n.617C>T
XR_001740353.2:n.617C>T
XR_924208.2:n.617C>T