Canonical Allele Identifier: CA1425881497
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184136668T= , CM000665.2:g.184136668T= GRCh38
NC_000003.11:g.183854456T= , CM000665.1:g.183854456T= GRCh37
NC_000003.10:g.185337150T= NCBI36
NG_015826.1:g.6647T=

Transcript Alleles

HGVS Amino-acid change
ENST00000432569.2:c.252T= ENSP00000414775.1:p.Thr84=
ENST00000465218.3:n.275T=
ENST00000468748.7:n.235T=
ENST00000471832.2:c.*246T= ENSP00000497786.1:n.*246T=
ENST00000491008.6:n.117T=
ENST00000492226.2:n.249T=
ENST00000647636.1:c.252T= ENSP00000497505.1:p.Thr84=
ENST00000647909.1:c.252T= ENSP00000498164.1:p.Thr84=
ENST00000648145.1:c.20T=
ENST00000648189.1:c.2T=
ENST00000648256.1:c.201T= ENSP00000497356.1:p.Thr67=
ENST00000648314.1:c.252T= ENSP00000496920.1:p.Thr84=
ENST00000648599.1:c.252T= ENSP00000497159.1:p.Thr84=
ENST00000648630.1:c.246T= ENSP00000497887.1:p.Thr82=
ENST00000648682.1:c.252T= ENSP00000498185.1:p.Thr84=
ENST00000648882.1:c.*78T= ENSP00000497603.1:n.*78T=
ENST00000648890.1:c.252T= ENSP00000497503.1:p.Thr84=
ENST00000648915.2:c.252T= MANE Select ENSP00000497160.1:p.Thr84=
ENST00000649688.1:c.252T= ENSP00000497097.1:p.Thr84=
ENST00000649814.1:n.301T=
ENST00000650244.1:c.397T= ENSP00000497227.1:n.397T=
ENST00000650270.1:c.119T=
ENST00000273783.7:c.252T= ENSP00000273783.3:p.Thr84=
ENST00000432569.1:c.252T= ENSP00000414775.1:p.Thr84=
ENST00000432982.5:c.238T=
ENST00000444495.1:c.252T= ENSP00000409142.1:p.Thr84=
ENST00000471832.1:n.183T=
ENST00000481054.5:n.253T=
ENST00000491144.5:n.600T=
ENST00000498831.1:n.108T=
NM_003907.2:c.252T= NP_003898.2:p.Thr84=
XR_924208.1:n.1203T=
NM_003907.3:c.252T= MANE Select NP_003898.2:p.Thr84=
XM_011513266.3:c.-650T= XP_011511568.1:n.-650T=
XR_001740352.2:n.615T=
XR_001740353.2:n.615T=
XR_924208.2:n.615T=