Canonical Allele Identifier: CA1425881493
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184136666A= , CM000665.2:g.184136666A= GRCh38
NC_000003.11:g.183854454A= , CM000665.1:g.183854454A= GRCh37
NC_000003.10:g.185337148A= NCBI36
NG_015826.1:g.6645A=

Transcript Alleles

HGVS Amino-acid change
ENST00000432569.2:c.250A= ENSP00000414775.1:p.Thr84=
ENST00000465218.3:n.273A=
ENST00000468748.7:n.233A=
ENST00000471832.2:c.*244A= ENSP00000497786.1:n.*244A=
ENST00000491008.6:n.115A=
ENST00000492226.2:n.247A=
ENST00000647636.1:c.250A= ENSP00000497505.1:p.Thr84=
ENST00000647909.1:c.250A= ENSP00000498164.1:p.Thr84=
ENST00000648145.1:c.18A=
ENST00000648256.1:c.199A= ENSP00000497356.1:p.Thr67=
ENST00000648314.1:c.250A= ENSP00000496920.1:p.Thr84=
ENST00000648599.1:c.250A= ENSP00000497159.1:p.Thr84=
ENST00000648630.1:c.244A= ENSP00000497887.1:p.Thr82=
ENST00000648682.1:c.250A= ENSP00000498185.1:p.Thr84=
ENST00000648882.1:c.*76A= ENSP00000497603.1:n.*76A=
ENST00000648890.1:c.250A= ENSP00000497503.1:p.Thr84=
ENST00000648915.2:c.250A= MANE Select ENSP00000497160.1:p.Thr84=
ENST00000649688.1:c.250A= ENSP00000497097.1:p.Thr84=
ENST00000649814.1:n.299A=
ENST00000650244.1:c.395A= ENSP00000497227.1:n.395A=
ENST00000650270.1:c.117A=
ENST00000273783.7:c.250A= ENSP00000273783.3:p.Thr84=
ENST00000432569.1:c.250A= ENSP00000414775.1:p.Thr84=
ENST00000432982.5:c.236A=
ENST00000444495.1:c.250A= ENSP00000409142.1:p.Thr84=
ENST00000471832.1:n.181A=
ENST00000481054.5:n.251A=
ENST00000491144.5:n.598A=
ENST00000498831.1:n.106A=
NM_003907.2:c.250A= NP_003898.2:p.Thr84=
XR_924208.1:n.1201A=
NM_003907.3:c.250A= MANE Select NP_003898.2:p.Thr84=
XM_011513266.3:c.-652A= XP_011511568.1:n.-652A=
XR_001740352.2:n.613A=
XR_001740353.2:n.613A=
XR_924208.2:n.613A=