Canonical Allele Identifier: CA1425882993
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138021C= , CM000665.2:g.184138021C= GRCh38
NC_000003.11:g.183855809C= , CM000665.1:g.183855809C= GRCh37
NC_000003.10:g.185338503C= NCBI36
NG_015826.1:g.8000C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.653C=
ENST00000468748.7:n.613C=
ENST00000484154.2:n.1251C=
ENST00000491008.6:n.1378C=
ENST00000492226.2:n.627C=
ENST00000492773.6:c.362C=
ENST00000647636.1:c.630C= ENSP00000497505.1:p.Asn210=
ENST00000647909.1:c.654C= ENSP00000498164.1:p.Asn218=
ENST00000648145.1:c.398C=
ENST00000648189.1:c.380C=
ENST00000648256.1:c.579C= ENSP00000497356.1:p.Asn193=
ENST00000648314.1:c.630C= ENSP00000496920.1:p.Asn210=
ENST00000648599.1:c.630C= ENSP00000497159.1:p.Asn210=
ENST00000648630.1:c.624C= ENSP00000497887.1:p.Asn208=
ENST00000648682.1:c.630C= ENSP00000498185.1:p.Asn210=
ENST00000648882.1:c.*456C= ENSP00000497603.1:n.*456C=
ENST00000648890.1:c.630C= ENSP00000497503.1:p.Asn210=
ENST00000648915.2:c.630C= MANE Select ENSP00000497160.1:p.Asn210=
ENST00000649545.1:c.364C=
ENST00000649688.1:c.630C= ENSP00000497097.1:p.Asn210=
ENST00000649814.1:n.679C=
ENST00000650270.1:c.497C=
ENST00000273783.7:c.630C= ENSP00000273783.3:p.Asn210=
ENST00000432982.5:c.245+1346C=
ENST00000444495.1:c.630C= ENSP00000409142.1:p.Asn210=
ENST00000468748.5:n.83C=
ENST00000481054.5:n.631C=
ENST00000491008.5:n.594C=
ENST00000491144.5:n.1070C=
ENST00000498831.1:n.585C=
NM_003907.2:c.630C= NP_003898.2:p.Asn210=
XR_924208.1:n.1581C=
NM_003907.3:c.630C= MANE Select NP_003898.2:p.Asn210=
XM_011513266.3:c.-272C= XP_011511568.1:n.-272C=
XR_001740352.2:n.993C=
XR_001740353.2:n.993C=
XR_924208.2:n.993C=