Canonical Allele Identifier: CA1425889732
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184144185C= , CM000665.2:g.184144185C= GRCh38
NC_000003.11:g.183861973C= , CM000665.1:g.183861973C= GRCh37
NC_000003.10:g.185344667C= NCBI36
NG_015826.1:g.14164C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.2278C=
ENST00000468748.7:n.3031C=
ENST00000484154.2:n.3018C=
ENST00000491008.6:n.2720C=
ENST00000492226.2:n.3055C=
ENST00000492773.6:c.1710C=
ENST00000647636.1:c.*805C= ENSP00000497505.1:n.*805C=
ENST00000647909.1:c.1980C= ENSP00000498164.1:p.Phe660=
ENST00000648145.1:c.1748C=
ENST00000648189.1:c.1790C=
ENST00000648256.1:c.1928C= ENSP00000497356.1:n.1928C=
ENST00000648314.1:c.*1345C= ENSP00000496920.1:n.*1345C=
ENST00000648599.1:c.*1239C= ENSP00000497159.1:n.*1239C=
ENST00000648630.1:c.2134C= ENSP00000497887.1:n.2134C=
ENST00000648682.1:c.*1095C= ENSP00000498185.1:n.*1095C=
ENST00000648882.1:c.*1782C= ENSP00000497603.1:n.*1782C=
ENST00000648890.1:c.*379C= ENSP00000497503.1:n.*379C=
ENST00000648915.2:c.1956C= MANE Select ENSP00000497160.1:p.Phe652=
ENST00000649545.1:c.1615C=
ENST00000649688.1:c.*1548C= ENSP00000497097.1:n.*1548C=
ENST00000649814.1:n.2554C=
ENST00000650270.1:c.1834C=
ENST00000273783.7:c.1956C= ENSP00000273783.3:p.Phe652=
ENST00000444495.1:c.1956C= ENSP00000409142.1:p.Phe652=
ENST00000465218.2:n.738C=
ENST00000481054.5:n.2882C=
ENST00000491144.5:n.2460C=
ENST00000492226.1:n.132C=
NM_003907.2:c.1956C= NP_003898.2:p.Phe652=
XM_011513265.1:c.1206C= XP_011511567.1:p.Phe402=
XM_011513266.1:c.1119C= XP_011511568.1:p.Phe373=
XR_924208.1:n.2923C=
NM_003907.3:c.1956C= MANE Select NP_003898.2:p.Phe652=
XM_011513266.3:c.1119C= XP_011511568.1:p.Phe373=
XR_001740352.2:n.2330C=
XR_001740353.2:n.2346C=
XR_924208.2:n.2335C=