Canonical Allele Identifier: CA1425882744
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137803C= , CM000665.2:g.184137803C= GRCh38
NC_000003.11:g.183855591C= , CM000665.1:g.183855591C= GRCh37
NC_000003.10:g.185338285C= NCBI36
NG_015826.1:g.7782C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.527C=
ENST00000468748.7:n.487C=
ENST00000484154.2:n.1125C=
ENST00000491008.6:n.1252C=
ENST00000492226.2:n.501C=
ENST00000492773.6:c.236C=
ENST00000647636.1:c.504C= ENSP00000497505.1:p.His168=
ENST00000647909.1:c.504C= ENSP00000498164.1:p.His168=
ENST00000648145.1:c.272C=
ENST00000648189.1:c.254C=
ENST00000648256.1:c.453C= ENSP00000497356.1:p.His151=
ENST00000648314.1:c.504C= ENSP00000496920.1:p.His168=
ENST00000648599.1:c.504C= ENSP00000497159.1:p.His168=
ENST00000648630.1:c.498C= ENSP00000497887.1:p.His166=
ENST00000648682.1:c.504C= ENSP00000498185.1:p.His168=
ENST00000648882.1:c.*330C= ENSP00000497603.1:n.*330C=
ENST00000648890.1:c.504C= ENSP00000497503.1:p.His168=
ENST00000648915.2:c.504C= MANE Select ENSP00000497160.1:p.His168=
ENST00000649545.1:c.238C=
ENST00000649688.1:c.504C= ENSP00000497097.1:p.His168=
ENST00000649814.1:n.553C=
ENST00000650244.1:c.649C= ENSP00000497227.1:n.649C=
ENST00000650270.1:c.371C=
ENST00000273783.7:c.504C= ENSP00000273783.3:p.His168=
ENST00000432982.5:c.245+1128C=
ENST00000444495.1:c.504C= ENSP00000409142.1:p.His168=
ENST00000481054.5:n.505C=
ENST00000491008.5:n.468C=
ENST00000491144.5:n.852C=
ENST00000498831.1:n.459C=
NM_003907.2:c.504C= NP_003898.2:p.His168=
XR_924208.1:n.1455C=
NM_003907.3:c.504C= MANE Select NP_003898.2:p.His168=
XM_011513266.3:c.-398C= XP_011511568.1:n.-398C=
XR_001740352.2:n.867C=
XR_001740353.2:n.867C=
XR_924208.2:n.867C=