Canonical Allele Identifier: CA1425889743
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184144189C= , CM000665.2:g.184144189C= GRCh38
NC_000003.11:g.183861977C= , CM000665.1:g.183861977C= GRCh37
NC_000003.10:g.185344671C= NCBI36
NG_015826.1:g.14168C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.2282C=
ENST00000468748.7:n.3035C=
ENST00000484154.2:n.3022C=
ENST00000491008.6:n.2724C=
ENST00000492226.2:n.3059C=
ENST00000492773.6:c.1714C=
ENST00000647636.1:c.*809C= ENSP00000497505.1:n.*809C=
ENST00000647909.1:c.1984C= ENSP00000498164.1:p.Leu662=
ENST00000648145.1:c.1752C=
ENST00000648189.1:c.1794C=
ENST00000648256.1:c.1932C= ENSP00000497356.1:n.1932C=
ENST00000648314.1:c.*1349C= ENSP00000496920.1:n.*1349C=
ENST00000648599.1:c.*1243C= ENSP00000497159.1:n.*1243C=
ENST00000648630.1:c.2138C= ENSP00000497887.1:n.2138C=
ENST00000648682.1:c.*1099C= ENSP00000498185.1:n.*1099C=
ENST00000648882.1:c.*1786C= ENSP00000497603.1:n.*1786C=
ENST00000648890.1:c.*383C= ENSP00000497503.1:n.*383C=
ENST00000648915.2:c.1960C= MANE Select ENSP00000497160.1:p.Leu654=
ENST00000649545.1:c.1619C=
ENST00000649688.1:c.*1552C= ENSP00000497097.1:n.*1552C=
ENST00000649814.1:n.2558C=
ENST00000650270.1:c.1838C=
ENST00000273783.7:c.1960C= ENSP00000273783.3:p.Leu654=
ENST00000444495.1:c.1960C= ENSP00000409142.1:p.Leu654=
ENST00000465218.2:n.742C=
ENST00000481054.5:n.2886C=
ENST00000491144.5:n.2464C=
ENST00000492226.1:n.136C=
NM_003907.2:c.1960C= NP_003898.2:p.Leu654=
XM_011513265.1:c.1210C= XP_011511567.1:p.Leu404=
XM_011513266.1:c.1123C= XP_011511568.1:p.Leu375=
XR_924208.1:n.2927C=
NM_003907.3:c.1960C= MANE Select NP_003898.2:p.Leu654=
XM_011513266.3:c.1123C= XP_011511568.1:p.Leu375=
XR_001740352.2:n.2334C=
XR_001740353.2:n.2350C=
XR_924208.2:n.2339C=