Canonical Allele Identifier: CA1425881499
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000432569.2:c.254C= ENSP00000414775.1:p.Ala85=
ENST00000465218.3:n.277C=
ENST00000468748.7:n.237C=
ENST00000471832.2:c.*248C= ENSP00000497786.1:n.*248C=
ENST00000491008.6:n.119C=
ENST00000492226.2:n.251C=
ENST00000647636.1:c.254C= ENSP00000497505.1:p.Ala85=
ENST00000647909.1:c.254C= ENSP00000498164.1:p.Ala85=
ENST00000648145.1:c.22C=
ENST00000648189.1:c.4C=
ENST00000648256.1:c.203C= ENSP00000497356.1:p.Ala68=
ENST00000648314.1:c.254C= ENSP00000496920.1:p.Ala85=
ENST00000648599.1:c.254C= ENSP00000497159.1:p.Ala85=
ENST00000648630.1:c.248C= ENSP00000497887.1:p.Ala83=
ENST00000648682.1:c.254C= ENSP00000498185.1:p.Ala85=
ENST00000648882.1:c.*80C= ENSP00000497603.1:n.*80C=
ENST00000648890.1:c.254C= ENSP00000497503.1:p.Ala85=
ENST00000648915.2:c.254C= MANE Select ENSP00000497160.1:p.Ala85=
ENST00000649688.1:c.254C= ENSP00000497097.1:p.Ala85=
ENST00000649814.1:n.303C=
ENST00000650244.1:c.399C= ENSP00000497227.1:n.399C=
ENST00000650270.1:c.121C=
ENST00000273783.7:c.254C= ENSP00000273783.3:p.Ala85=
ENST00000432569.1:c.254C= ENSP00000414775.1:p.Ala85=
ENST00000432982.5:c.240C=
ENST00000444495.1:c.254C= ENSP00000409142.1:p.Ala85=
ENST00000471832.1:n.185C=
ENST00000481054.5:n.255C=
ENST00000491144.5:n.602C=
ENST00000498831.1:n.110C=
NM_003907.2:c.254C= NP_003898.2:p.Ala85=
XR_924208.1:n.1205C=
NM_003907.3:c.254C= MANE Select NP_003898.2:p.Ala85=
XM_011513266.3:c.-648C= XP_011511568.1:n.-648C=
XR_001740352.2:n.617C=
XR_001740353.2:n.617C=
XR_924208.2:n.617C=